medical information

25 years of Providing World-Class Medical Information Services.

Medical information flywheel heading logo.
Medical information flywheel heading mobile logo.
Colorized half circle.
Medical information consultant in front of medical information flywheel icon

Comprehensive Medical Information and Contact Center Services

With strategically positioned and seamlessly integrated contact centers around the world, we provide customizable medical information services to meet the needs of companies of all sizes. Whether you need medical information, patient support, commercial inquiry handling, or other extended medical information services, our team of medical information specialists have the knowledge and experience to effectively support your needs.

Medical Information and Global Contact Center Solutions:

Our innovative, market-leading technologies, and 24/7/365 contact centers allow us to provide best-in-class medical information services.

 

Global Contact Center Support

A global contact center plays a vital role in ensuring consistent service, accessing global talent, offering multilingual support, establishing scalability, providing 24/7 availability, and maintaining redundancy and disaster recovery capabilities. Our contact center empowers our clients to efficiently and effectively deliver Medical Information, Patient Support, and Commercial services, allowing them to cater to the needs of a global customer base. Simultaneously, it helps them achieve cost savings and enhance their competitiveness in the global marketplace.

Medical Information support personnel wearing headsets

 

Bilingual Native Speakers

Our team of highly trained specialists includes bilingual native speakers in more than 35 languages. With globally integrated contact centers around the world, we can respond to product inquiries in a manner that is not only consistent with product labeling and regulatory guidance, but also consistent with local evidence, culture, and communication styles.

Explore Global Contact Center Services

Medical Information

ProPharma has 25 years of expertise in delivering Medical Information services to our clientele. We specialize in distributing vital information regarding our clients' healthcare products to healthcare professionals, patients, and the wider public. Our dedicated team consists of seasoned healthcare professionals (HCPs) and graduates in life sciences who function as an integral part of your team, facilitating the exchange of clinical and scientific information related to drugs and devices, as well as product safety. Medical Information is a vital component that ensures the safe and effective use of healthcare products, supports healthcare professionals in their practice, and helps pharmaceutical and biotech companies comply with regulatory requirements.

Talk to an Expert

Technology Enablement

In Medical Information, we are integrating advanced technological tools such as AI to enhance the efficiency and quality of our services. By embedding these technologies into our workflow, we enable patients and healthcare providers to reach us more quickly, allowing our team to promptly deliver necessary information with improved service quality. We adopt the co-pilot concept, where AI assists our MI specialists to be more efficient, while our specialists meticulously review AI’s work for accuracy, completeness, and compliance before delivering it to patients and healthcare providers. This synergistic approach not only accelerates response times and improves service quality but also ensures patient safety through human oversight. As we continue to evolve with technological advancements, we remain committed to providing reliable medical information services.

Adverse Event Intake and Follow-up Services

ProPharma's Medical Information (MI) team is trained on Adverse Event (AE) intake since onboarding as part of MI processing. We ensure that every AE is collected for patients' safety, customer journey, and compliance at every contact center exchange and sent to the designated pharmacovigilance (PV) department. For a seamless experience, ProPharma offers comprehensive AE processing and reporting through our dedicated PV team to supplement or fully outsource your existing PV function.

Comprehensive AE Intake

Our skilled specialists follow established global processes and guidelines to obtain timely, accurate, and comprehensive AE information. ProPharma conducts refresher training, regular updates, and quality monitoring to ensure that every AE is detected and delivered to PV within 1 business day. Our AE collection forms can be customized for your needs in our fully validated database and our specialists are experienced with various client databases and AE forms.

Man showing co-worker something on their computer monitor

Adverse Event Follow-up

Our experienced MI team is fully equipped to execute outbound follow-up communication and collect additional data that was not available at initial intake, which lessens the burden on your pharmacovigilance department.

Seamless Integration to Pharmacovigilance

All AE records automatically migrate from MI to the PV database within ProPharma, and you can review and monitor all cases from beginning to end in a single-point access 24/7. ProPharma can also integrate (E2B) with your PV database for the seamless and timely transfer of AE records.

Talk to an Expert

Product Complaint Intake and Follow-Up Services

ProPharma's MI team is trained on Product Quality Complaint (PQC) intake since onboarding as part of MI processing. We ensure that every PQC is collected for patients’ safety, customer journey, and compliance at every contact center exchange and sent to the designated quality department. We are dedicated to supporting your customers and patients by handling every PQC and your company’s reputation with empathy and care.

Comprehensive PQC Intake

As your trusted MI partner, our highly trained specialists follow established global processes and guidelines for handling PQC events, to meet regulatory reporting requirements as well as your company’s own internal quality and manufacturing standards. ProPharma conducts refresher training, regular updates, and quality monitoring to ensure that every PQC is detected and delivered to the quality department within 1 business day. Our PQC collection forms can be customized for your needs in our fully validated database and our specialists are experienced with various client databases and PQC forms.

Physician using a tablet

Global Quality Serialization and Product Surety

We work collaboratively with our clients to offer centralized solutions for Global Quality Serialization and Product Surety (Level 5 Alerts), compliant with EU FMD and US DSCSA. Our skilled staff have extensive experience with the alerts that are generated within the European Medicines Verification System (EMVS), detected by a national system, which are escalated to other stakeholders, including National Competent Authorities (NCAs) as they are generated. Our experienced team are also fully equipped to follow the process requirements for triage, follow-up, and closure of any Product Quality Serialization Verification requests. The intent of the requirements for reporting Level 5 Alerts set out in the Falsified Medicines Directive is to protect patient safety. Therefore, we ensure that our approach is pragmatic, effective, efficient, and solely focused on you and your patients.

Explore DSCSA Compliance and Serialization Services
Medcial professional using laptop

Product Retrieval

Our specialists communicate product retrieval instructions as well as company policies regarding product replacement or reimbursement requests. We can also create a product retrieval kit and logistics to provide to the customers to return the products to your quality department or manufacturer.

Talk to an Expert

Patient Support and Commercial Services

ProPharma offers extensive Patient Support and Commercial Services to support our clients' customers and patients to provide bespoke, best-in-class global Patient Support around the world. Our diverse team of global contact centers and certified field partners support patients and healthcare professionals worldwide in obtaining, understanding, and adhering to therapies for a well-rounded customer journey.

Explore Patient Support Services

Health professional assisting a patient with a mobile device

 

Medical Writing, Content Management & Translation

Medical writing is an essential part of scientific information exchange, which requires expert knowledge to analyze and prepare a variety of clinical and patient documents.

Our team of writers, editors, and quality reviewers knows what it takes to produce clear, concise text for your clinical, scientific, and regulatory needs.

Standard Document Creation

Our query management services include developing and updating libraries of standard response documents, sourcing and supplying clinical papers, and writing safety summaries. Our team of bilingual, native-speaking medical professionals can create or translate key standard documents in more than 35 local languages.

Custom Response and Content Management

Clients turn to ProPharma for quality and affordable custom response documents, delivered in a timely manner. Our team has experience in all therapeutic areas, with backgrounds in both the life science industry and academia. We provide a full range of content services, including literature research, writing custom response documents, and adapting documentation for use in other geographies.

Response Document Maintenance

We understand the importance of keeping your documents up to date with strict version control to provide the most accurate responses to inquiries. We work with your teams to take this burden off your hands, with efficient document management processes that our clients trust and rely on.

Translation and Localization Services

We support your internal teams by creating new standard response documents, generating custom responses, and translating existing global and/or regional documents into one of over 35 supported languages. Our knowledgeable staff of bilingual native speakers leverage their extensive medical and communications experience to create effective documents that are consistent with local evidence, culture, and communication styles.

Tablet and stethoscope on a table

Other Medical Writing Services

From general guidance on strategy and formatting to specific projects — we can support your organization and adapt to changing needs.

  • Project compilation, hyperlinking, and publishing
  • Comprehensive project management
  • Content editing and proofreading: Including a QC review of data against text and source documents
  • Style guide and template creation
  • Literature searches, analysis, reference libraries, and citations
  • Standard operating procedure (SOP) development
  • Abstracts, Manuscripts, and White Papers
  • Patient Education
  • Informed Consent forms
  • Clinical Study Reports (CSRs) and narratives
  • Publication strategy


Talk to an Expert

Animal Health Medical Information & Pharmacovigilance Services

ProPharma provides comprehensive Animal Health Medical Information (MI) and Pharmacovigilance (PV) support services, including expertise with the multiple regulatory environments that varied species and active ingredients require. ProPharma’s Animal Health team includes experienced veterinarians, pharmacists, veterinary technicians, and other healthcare professionals who ensure the highest levels of compliance. This enables us to respond to medical inquiries in a manner that is not only consistent with product labeling and regulatory guidance but also recognizes the connection between animals and people and the importance of communication between interdisciplinary healthcare professionals. ProPharma’s team of experts provides a customized solution to fit the Animal Health MI and PV needs of companies of all sizes. Whether you need to augment your internal team or need to completely outsource the Animal Health MI or PV functions globally, ProPharma has the right solution for your specific needs.

Healthcare professional writing on clipboard next to a laptop

 

Animal Health & Toxicology Medical Information Contact Center

  • Global 24/7/365 contact center support on Medical Information inquiry fulfillment, escalation, Adverse Event/Product Complaint intake and follow-up services 
  • Accidental exposure triage with toxicology assessment and follow-up services 
  • Crisis detection and client emergency bullhorn actions

Animal Health Pharmacovigilance Services

  • Adverse Drug Experience (ADE) assessment and processing
  • FDA Center for Veterinary Medicine (FDA CVM) ADE report preparation and review 
  • Signal detection and management 
  • Single service integration of non-FDA product regulatory needs including but not limited to NASC, EPA/FIFRA, USDA, and Health Canada/PMRA 

Leading Medical Information and Contact Center Services for Over 25 Years

ProPharma has been expanding medical information and contact center services since 1994 through partnership, leveraging new acquisitions, and building creative solutions at the intersection of talent and capabilities.

1994

1997

1998

2000

2011

2014

2015

2018

Founded

Prosar

Toxicology Call Center providing Animal Services and Medical Information in the United States.

Founded

SOLUTIONS in Health

Established as a leader in Canadian Medical Information services.

Founded

Professional Information Ltd.

Delivering Medical Information services in Europe and APAC.

Founded

Advanced Response Management (ARM)

Delivering Medical Information services in the Unites States.

Acquired

Advanced Response Management (ARM)

Expanded ProPharma’s suite of services to include Medical Information based in the United States.

Acquired

Professional Information Ltd.

Professional Information Ltd. joined ProPharma, expanding medical information services across Europe and APAC.

Acquired

Prosar

Prosar joined ProPharma, continuing to grow our excellence in call center services.

Acquired

SOLUTIONS in Health

SOLUTIONS in Health joined ProPharma, expanding our services to Canada.

1994

Click here to expand this section

Founded

Prosar

Toxicology Call Center providing Animal Services and Medical Information in the United States.

1997

Click here to expand this section

Founded

SOLUTIONS in Health

Established as a leader in Canadian Medical Information services.

1998

Click here to expand this section

Founded

Professional Information Ltd.

Delivering Medical Information services in Europe and APAC.

2000

Click here to expand this section

Founded

Advanced Response Management (ARM)

Delivering Medical Information services in the Unites States.

2011

Click here to expand this section

Acquired

Advanced Response Management (ARM)

Expanded ProPharma’s suite of services to include Medical Information based in the United States.

2014

Click here to expand this section

Acquired

Professional Information Ltd.

Professional Information Ltd. joined ProPharma, expanding medical information services across Europe and APAC.

2015

Click here to expand this section

Acquired

Prosar

Prosar joined ProPharma, continuing to grow our excellence in call center services.

2018

Click here to expand this section

Acquired

SOLUTIONS in Health

SOLUTIONS in Health joined ProPharma, expanding our services to Canada.

Medical Information and Contact Center Global Footprint

US and Canada UK and Europe Asia Pacific

North America

Europe

Asia Pacific

Raleigh (HQ) 

107 West Hargett St.
Raleigh, NC 27601

1-888-242-0559

Philadelphia 

501 W. Office Center Dr, Suite 350
Fort Washington, PA 19034

1-888-242-0559

Windsor 

3000 Temple Dr, Suite 200
Windsor, ON N8W 5J6

1-519-252-9555

Berlin

Siemensdamm 62
13627 Berlin

+49 (0) 30 85606878 - 0

North Yorkshire 

Olliver, Aske, Richmond
North Yorkshire, DL10 5HX

+44 (0)1748 828800

Melbourne

Suite 6, Ground Level
452 Johnston Street
Abbotsford, VIC 3067

+61 3 8814 7900

Hyderabad 

3rd Block, 7th Floor,
My Home Hub, Madhapur, Patrika Nagar, HITEC City,
Hyderabad, Telangana 500081

+91 966 611 1980

Tokyo

5-27-5 Sendagaya, Shibuya-ku (suite 13-101, 13-102, 13-113, 13-130)

+81 3 6277 4041

Makati City

7th Floor Office F
Armstrong Corporate Center
HV Dela Costa Ave.
Salcedo Village
Makati City

+61 38814 7900

Shanghai

138 HuaiHai Zhong Lu
3F
Huangpu District
Shanghai

+61 38814 7900

Medical Information and Contact Center Global Footprint

US and Canada

Down arrow - click here to expand section.
Raleigh (HQ) 

107 West Hargett St.
Raleigh, NC 27601

1-888-242-0559

Philadelphia 

501 W. Office Center Dr, Suite 350
Fort Washington, PA 19034

1-888-242-0559

Windsor 

3000 Temple Dr, Suite 200
Windsor, ON N8W 5J6

1-519-252-9555

UK and Europe

Down arrow - click here to expand section.
Berlin

Siemensdamm 62
13627 Berlin

+49 (0) 30 85606878 - 0

North Yorkshire 

Olliver, Aske, Richmond
North Yorkshire, DL10 5HX

+44 (0)1748 828800

Asia Pacific

Down arrow - click here to expand section.
Melbourne

Suite 6, Ground Level
452 Johnston Street
Abbotsford, VIC 3067

+61 3 8814 7900

Hyderabad 

3rd Block, 7th Floor,
My Home Hub, Madhapur, Patrika Nagar, HITEC City,
Hyderabad, Telangana 500081

+91 966 611 1980

Tokyo

5-27-5 Sendagaya, Shibuya-ku (suite 13-101, 13-102, 13-113, 13-130)

+81 3 6277 4041

Makati City

7th Floor Office F
Armstrong Corporate Center
HV Dela Costa Ave.
Salcedo Village
Makati City

+61 38814 7900

Shanghai

138 HuaiHai Zhong Lu
3F
Huangpu District
Shanghai

+61 38814 7900

Medical Information Experts

  • Rajul Jain Bio Photo

    Rajul Jain

    President, Medical Information

    View Bio

  • Dave Bezick Bio Photo

    Dave Bezick

    Director, Medical Information

    View Bio

  • Hannah Hunter Bio Photo

    Hannah Hunter

    Director, Medical Information

    View Bio

  • Katie Tonge Bio Photo

    Katie Tonge

    Director, Medical Information

    View Bio

  • Leanne Shaw Bio Photo

    Leanne Shaw

    Senior Director, Medical Information

    View Bio

  • Valerie Huh Bio Photo

    Valerie Huh

    Director, Global Innovation and Implementation

    View Bio

  • Victoria Evans Bio Photo

    Victoria Evans

    Director, Medical Information

    View Bio

  • Eric Brandon Bio Photo

    Eric Brandon

    Director, Patient Services & Contact Center Operations

    View Bio

Rajul Jain has over 19 years of international experience in Medical Information (MI), Pharmacovigilance (PV), Technology, and Program Management. With an extensive educational background including an MBA, Engineering degree, PMP, Medical Affairs Competency Certificate (ACMA), and various other healthcare certifications, she brings a wealth of knowledge to her roles. She is currently President of Medical Information in ProPharma with responsibility for oversight and expansion of global contact center operations. Prior to this, she managed all of the MI programs for IQVIA and technology and automation solutions for MI/PV programs. Rajul is passionate about improving business processes and fostering innovative solutions in the healthcare and pharmaceutical industry.

Dave brings over 14 years of Medical Information Contact Center Management and Operations experience. A licensed Registered Nurse, Dave began his career as a front-line Medical Information Specialist and has continually advanced into roles of increasing responsibility within the Medical Affairs industry. Dave is currently the Senior Director of Americas Medical Information Service Delivery (Operations and Account Management) at ProPharma. Dave’s passion for the patient and HCP experience is evident in his approach to staff selection, employee development and operational excellence of his teams.
Hannah is the Director of Medical Information (MI), Europe at ProPharma, where she leads dedicated client services across the continent. With 16 years of experience in Medical Information, Hannah has supported pharmaceutical companies globally. She is passionate about the evolution of MI to better meet the needs of customers and clients. As a proven leader, Hannah excels in guiding and inspiring her team to achieve excellence. She places a strong emphasis on the provision of telephone-based MI, recognizing its importance as the primary channel for MI inquiries and its potential for excellent service delivery. Additionally, she is focused on leveraging technology to enhance the efficiency and effectiveness of medical information teams.
Katie has over 15 years of Medical Information outsourcing experience, as well as contact centre management, and is passionate about using Medical Information to improve the health and safety of patients. She enjoys working with clients to suggest innovative and commercially sustainable options for their Medical Information needs. She has a track record of establishing service levels and KPIs with clients to ensure the highest standards for customers.  She also has Project Management experience in helping clients transition from in-sourced services to an outsourced Medical information solution.
Leanne brings 14 years of Medical Information Contact Center Management and Operations experience across Europe and Asia Pacific. Leanne begun her career in this space as a UK Medical Information Specialist and has continually advanced into roles of increasing responsibility including client management, operations management, and project leadership. Leanne is currently the Senior Director of Medical Information Services for JAPAC at ProPharma. Leanne’s key focus on service evolution and customer excellence helps deliver JAPAC services to the highest standard of success.

Valerie Huh brings over 20 years of experience in the pharmaceutical and healthcare industries, with expertise in global operations and process improvements. She holds a Doctor of Pharmacy (Pharm.D.), a degree in Chemistry, and an MBA with a certificate in business analytics. In her current role, she leads innovation and technology enablement in Medical Information and supports business expansions, driving forward strategic initiatives to enhance service quality and operational efficiency.

Victoria Evans is a seasoned professional with over nine years of experience in the Medical Information (MI) field. As the Director of Client Services at ProPharma, she leads a global team of Implementation and Client Account Managers, ensuring the successful onboarding, implementation, and maintenance of MI clients worldwide. Victoria holds a BSc in Psychology and has furthered her education with a Graduate Diploma in Law and a Legal Practice Certificate. Her passion for project management and patient safety drives her to find innovative solutions, and her focus and excellent project skills consistently help clients achieve their goals.

Eric has spent 30+ years in the pharmaceutical industry with the last 12 years striving to make a difference in Patient Services on the manufacturer side, as a consultant, and as a leader on the supplier side. As Director, Patient Services & Contact Center Operations he leads the strategy and oversight for global and regional Patient Support Programs (PSPs), Commercial Services, Clinical Trial Support, and other Global contact center-based programs.

He has a great passion for supporting patients wherever they are in their clinical trial or treatment journey. Eric inspires his team to focus on the patient and their specific needs to ensure they get the right support throughout their treatment journey, including insurance benefits verification, financial support, device training and support, concierge travel assistance and other innovative services. More importantly, we are here to provide the right level of professional resources to support patients through their treatment journey to ensure their safety and improve their health.

News & Insights

GxP Readiness and Auditing: Your Quality System’s Insurance Policy for Compliance Systems

November 4, 2024

GxP Readiness and Auditing: Your Quality System’s Insurance Policy for Compliance Systems

GxP readiness and internal audits ensure compliance, safeguarding organizations by mitigating risks, saving costs, and providing peace of mind.

EU Clinical Trials Regulation: Time Is Running Out, Are You Ready?

October 31, 2024

EU Clinical Trials Regulation: Time Is Running Out, Are You Ready?

Prepare for the EU Clinical Trials Regulation (CTR) deadline: transition ongoing trials from EU-CTD to CTR by January 2025 to ensure compliance.

Navigating the Nordic Pharmaceutical Landscape: Key Considerations for a Successful Launch

October 28, 2024

Navigating the Nordic Pharmaceutical Landscape: Key Considerations for a Successful Launch

Learn key strategies for regulatory compliance, quality assurance, and market access to ensure a successful product launch in the Nordics.

ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Names Dawn Sherman Chief Executive Officer

September 30, 2024

ProPharma Names Dawn Sherman Chief Executive Officer

Dawn Sherman rejoins ProPharma as CEO, bringing nearly 30 years of industry experience to lead the regulatory, clinical, and compliance services provider.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

ProPharma Receives 2024 CRO Leadership Award

June 13, 2024

ProPharma Receives 2024 CRO Leadership Award

ProPharma wins 2024 CRO Leadership Award for exceeding expectations in key categories, solidifying its position as a top global research consulting organization in the life sciences industry.

Infographic The Cost of Poor Project Management - ProPharma

June 10, 2022

The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...

Infographic Successfully Passing MHRA Inspections for Overseas Manufacturing Sites - ProPharma

August 31, 2022

Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...

Infographic Navigating the Generic Drug Application and Approval Process - ProPharma

October 4, 2021

Navigating the Generic Drug Application and Approval Process

Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...

News & Insights

ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Names Dawn Sherman Chief Executive Officer

September 30, 2024

ProPharma Names Dawn Sherman Chief Executive Officer

Dawn Sherman rejoins ProPharma as CEO, bringing nearly 30 years of industry experience to lead the regulatory, clinical, and compliance services provider.

Previous Post Arrow Next Post Arrow
ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

ProPharma Receives 2024 CRO Leadership Award

June 13, 2024

ProPharma Receives 2024 CRO Leadership Award

ProPharma wins 2024 CRO Leadership Award for exceeding expectations in key categories, solidifying its position as a top global research consulting organization in the life sciences industry.

Previous Award Arrow Next Award Arrow
GxP Readiness and Auditing: Your Quality System’s Insurance Policy for Compliance Systems

November 4, 2024

GxP Readiness and Auditing: Your Quality System’s Insurance Policy for Compliance Systems

GxP readiness and internal audits ensure compliance, safeguarding organizations by mitigating risks, saving costs, and providing peace of mind.

EU Clinical Trials Regulation: Time Is Running Out, Are You Ready?

October 31, 2024

EU Clinical Trials Regulation: Time Is Running Out, Are You Ready?

Prepare for the EU Clinical Trials Regulation (CTR) deadline: transition ongoing trials from EU-CTD to CTR by January 2025 to ensure compliance.

Navigating the Nordic Pharmaceutical Landscape: Key Considerations for a Successful Launch

October 28, 2024

Navigating the Nordic Pharmaceutical Landscape: Key Considerations for a Successful Launch

Learn key strategies for regulatory compliance, quality assurance, and market access to ensure a successful product launch in the Nordics.

Previous Post Arrow Next Post Arrow
Infographic The Cost of Poor Project Management - ProPharma

June 10, 2022

The Cost of Poor Project Management

Project Management isn’t for the faint of heart. There is a shockingly high rate of project failure… but on the other hand, great project management can be a key differentiator that leads a company...

Infographic Successfully Passing MHRA Inspections for Overseas Manufacturing Sites - ProPharma

August 31, 2022

Successfully Passing MHRA Inspections for Overseas Manufacturing Sites

ProPharma offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. ProPharma’s Compliance and Quality team completed the first on-site...

Infographic Navigating the Generic Drug Application and Approval Process - ProPharma

October 4, 2021

Navigating the Generic Drug Application and Approval Process

Navigating the generic drug application and approval process can be challenging. From pre-filing through post-approval, find out exactly what needs to be done for your Abbreviated New Drug...

Previous Resource Arrow Next Resource Arrow
Gradient Image

Complex Needs Require Custom Solutions

ProPharma builds solutions at the intersection of innovation and flexibility. We’re here to offer a custom alternative that fits your unique needs. Standout solutions scaled to your size.