David Crome

MSc, MBA, DBA,

With over 45 years of experience in the pharmaceutical industry, David Crome has worked with both branded and generic multinational companies, including a decade in consultancy. His career has spanned most functions in the industry, covering the entire product lifecycle: R&D, regulatory, production, QA, supply chain, auditing (with over 150 audits undertaken), marketing, setting up new businesses, and assisting clients in attaining EU/UK GMP certification. David has participated in over 60 regulatory inspections conducted by various agencies, such as the MHRA, HPRA, EMA, SUKL, USFDA, SAHPRA, and Anvisa, across England, Ireland, Argentina, Bangladesh, the Czech Republic, and India.

Quality & Compliance

EU Pharmaceutical Legislation Revisions FAQ

On April 26, 2023 the Commission adopted a proposal for a new Directive and a new Regulation which revise and replace the existing general pharmaceutical legislation under the following...

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