Trident BioPharm Solutions

Trident BioPharm is a boutique life science consultancy engaged in helping biopharm organization create enterprise value, increase efficiencies and reduce time to market. The team at Trident brings  highly experienced consultants with deep domain expertise in the economic, scientific, regulatory and organisational issues across the pharma development life cycle and deliver a cross–disciplinary approach to solve complex problems for clients.

Managing Director

Proclinical Consulting

We deliver on every stage of the life science process to help you grow faster by providing our partners with end-to-end strategic, operational and commercial guidance to develop, register and launch products

Director - Proclinical Consulting

PAREXEL

Project Leader - Programme Managment

Covance

Regulatory Submissions Manager

AMCo (Formerly Amdipharm Mercury Ltd)

Senior Regulatory Executive

Teva Pharmaceuticals

Preparation / Maintenance of EU abridged MAA dossiers (MRP, DCP, CP)

Regulatory Affairs Officer

Allergan

Regulatory Affairs Lead

Amdipharm

Assisting in the review and management of regulatory compliance/submission strategies for Amdipharm PLC’s portfolio of pharmaceutical products.

Supporting Life Cycle Management (CMC) activities for National / MRP licences.

Regulatory Affairs Executive

World Intellectual Property Organization – WIPO

•Gained a World Intellectual Property Organisation (WIPO) accreditation for completing and passing the General Course in Intellectual Property (DL-101). 
•Selected to attend the competitive WIPO summer school internship on IP in Geneva, Switzerland
•Acquired a thorough understanding of IP as it relates economic, social, cultural and technological development worldwide
•Broad exposure to emerging areas in IP including its impact on Food security, Biodiversity, Climate change and Public health.
•Familiarity with WIPO administered treaties and their role in obtaining IP protection globally

United Nations

•Expertise gained in assessing the safety profile of drugs by characterising potential undesirable pharmacodynamic effects on the cardiovascular, pulmonary and central nervous systems.

Safety Pharmacologist

Tox Operations - Early Development

Experienced Commercial Director with a hands-on background in Biopharm Consulting, Business Transformation, Regulatory Affairs and Strategic Project/Portfolio Management activities. Excellent grasp of regulatory requirements in the development of therapeutics, vaccines and medical devices

Operating within the Pharmaceutical Services market I founded Trident BioPharm Solutions where we provide a tailored, innovative solutions for key problems facing biopharm and medical device companies across the development life cycle, from inception to market.

Specialities: Leadership, Project management, Consulting, Business development, Strategy,  Regulatory Affairs (Pre and Post Approval),  Drugs Licensing and Compliance, Life Cycle Management, Broad General Regulatory experience across the GxP’s, Drug Safety, Quality Assurance, Technical Transfer, Clin & Non Clin, Biometrics, Commercial Operations

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