Helping to bring medicines and other healthcare products to people quicker

Welcome to CAMPHARM

We are an International regulatory affairs and development Consultancy Company for Pharmaceutical and other Healthcare Companies. Founded in 2005, CAMPHARM is building its regulatory and development services through an already strong foundation from previous experience of working with many pharmaceutical healthcare companies as well as CROs and smaller consultancies. CAMPHARM can guide and support you through the maze of regulatory requirements and development activities with solutions to bring your products to your customers faster.

With over 20 years of drug development and regulatory affairs internal broad regulatory and drug development experience, and a network of regulatory and consultant companies you are in capable hands to make the right decisions for your products that we know are very important to you and you would like to get to market quickly and efficiently.

CAMPHARM is an International regulatory affairs and drug development Consultancy Company for pharmaceutical, biotechnology and other healthcare companies

Take a look at the services that CAMPHARM can offer to your business more…

Who We Are
CAMPHARM Ltd has a network of Consultants and Companies that we work with to deliver the right solution for your needs more…

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  • I have worked with a number of regulatory consultants in both the US and EU. It is very challenging to find the perfect combination of expertise, accessibility, and strong judgment that is required to assist a small company through complicated and critical regulatory milestones. However, CAMPHARM, and particular Craig McCarthy, meets all of these requirements and has been our trusted advisor throughout the process of filing Clinical Trial Applications for our first global phase 3 trial, and now our first MAA submission. I would not hesitate to recommend CAMPHARM.–Vice President, Regulatory Affairs, Startup SME, Central, USA

  • As a small US-based start-up biopharmaceutical company, we searched for a company capable of providing European regulatory expertise from the initial filing of our clinical trial applications to submission of our Marketing Authorisation Application. CAMPHARM helped us remendously in developing and implementing the regulatory strategy for our unique product which is now awaiting approval. We benefited tremendously from CAMPHARM’s experience and familiarity with the different EU health authorities’ perspectives. Our experience with CAMPHARM has been extremely positive and I highly recommend them for all their regulatory needs.–Senior Vice President, Regulatory and Medical Affairs, Startup SME, South East, USA

  • For a middle size Japan-based Pharmaceutical company specialising in topical preparations, there were so many and unbelievably high and difficult regulatory barriers for us to enter the European market. Then, we appointed CAMPHARM as our European Regulatory representative for our National Marketing Authorisation Application of one of our newly developed products which was in a new category in the UK. Throughout this application, CAMPHARM provided us with their unique and strategically effective ideas with the right follow up actions to regulatory issues from their vast experience. Then, eventually, the desired National Marketing Authorisation was granted by the MHRA.  We deeply appreciate their professionalism and in the future, we will be asking CAMPHARM to progress our further Multinational Procedures.
    From our above mentioned experiences, we strongly recommend all international pharmaceutical companies who are intending to enter the European market to appoint CAMPHARM as your European Regulatory Representative if you really want to get approvals in the EU.–Senior Manager, International Division in Middle-size pharmaceutical company, Japan

  • We had searched months for a knowledgeable and responsive consultant to represent us with the European regulatory authorities.
    We found Craig McCarthy of CAMPHARM who turned out to be a critical asset in positioning and presenting our product to the regulatory authorities.
    He represented us in person, as well as telephonically. He was not only well prepared and professional, but most importantly was able to obtain the results we sought.
    We are also pleased to have him represent us with prospective buyers of our product and look forward to a long term relationship with him.
    –CEO, Small Pharmaceutical Company, South West Coast, USA