We support you through the life-cycle of your pharmaceutical and medical device products, building a medical team which translates strategic priorities into practical goals.

Once your product is launched PharmaMedic can work with you where needed to amend the licence and help develop, review and certify marketing and sales materials.  Working with generic companies we can develop a brand strategy based on recent data and a review of differences in comparable product’s Summaries of Product Characteristics (SmPCs).

Our expertise includes:

  • Advanced regulatory strategy
  • Pharmacovigilance services
  • On-going development of marketing and sales materials
  • Training material development
  • Code complaint defense
  • International representation with regulatory authorities
  • Final signatory/material compliance support
  • Development of branded materials for generic products
  • Transfer of licence from prescription-only medicine (POM)
    to pharmacy licence (P)

Case Study

A generic company with a well-established pipeline of products required a number of these assets to be marketed as branded products. PharmaMedic worked with the Company’s regulatory team and senior management to review the product’s SmPC’s/ data sets and find indications / particular aspects of the product which were unique to comparative products.

Branded marketing materials were developed with the client Team and branding allowed the Company to stand out against their competitors and gain a heightened market share and increased product awareness.

What Our Clients Say About Us

“Malcolm and his team bring years of world class experience covering the full range of expertise that one could possibly need within the pharmaceutical sector.  In short, outstanding.”
Dr Kathrine Scott, Medical Director at Gedeon Richter UK Ltd

Get in Touch

If you are a Company or Team looking to work with PharmaMedic Consultancy or you wish to discuss our services, please contact us.

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