Why i-Pharm Consulting Services?

With over 12 years’ experience meeting business-critical GxP needs for our partners, our network of technical experts will work with you to scope your requirements, identify key risks and opportunities, and agree on milestones for successful delivery.

We believe that every challenge is unique, which is why we adopt a tailor-made solution for each engagement; creating a roadmap for delivery that is purpose-built to your specific needs. I-Pharm Consulting meets all requirements in-house, eliminating complex supply chains and increasing value.

Click here for project example


When to consider i-Pharm Consulting Services?

If your business is experiencing significant change which requires a timebound, coordinated, and milestone-led solution, involving niche resources potentially in numerous locations, you can rely on us to deliver the right response. 

Previous examples have included upgrading equipment and technology, transferring production to an additional or new site, responding to time critical external audits, decommissioning an existing facility, or launching a new product or service. 

Click here to view our areas of expertise

What do you get?



Our capabilities:



How we do it.

Our model enables us to execute work-packages that range from large, complex global programmes to smaller, targeted initiatives.

All our services are outcomes-focused and are overseen by an expert leadership team, combining decades of experience operating within and alongside regulatory bodies such as the FDA and MHRA.

i-Pharm can deploy turnkey teams remotely, via secure technology, or on-site, via global workforce solutions, as required.


Our specialisms.


Our experienced Commercial recruitment team recruit across a range of disciplines including CRO Business Development, Pharmaceutical, Biotechnology, Medical Device companies.

Clinical Operations & Project Management

Clinical Operations & Clinical Trials Project Management is at the heart of what we do. We support some of the world’s largest CROs and Bio-Pharmaceutical companies with staffing for international clinical trials across Phases I to IV. 


We are experts at recruiting in the ever-changing and complex field of Biometrics. Example Roles: Statistical Programmers / SAS Programmers, Statisticians / Biostatistician, Clinical Data Managers, Data Scientists, Epidemiology, Heads of Department

Regulatory Affairs

Recruiting Regulatory Affairs professionals across Clinical Trials, CMC, Post-Licensing, Labelling, Medical Devices to support the development of New Chemical Entities, Biologics and Medical Devices for some of the sector’s best-known companies.


Our experienced Medical Affairs recruitment team specialises in roles across a range of Pharmaceutical, Biotechnology, CRO and Medical Devices organisations. 

Drug and Product Safety

We have a team dedicated to specialist Drug Safety / Pharamcovigilance Associates, Drug Safety / Pharamcovigilance Managers & Directors, Heads of Department and Drug Safety Physicians.

Clinical Development

Clinical Development, or Drug Development, is the process of bringing a drug to the market. At i-Pharm, we support our clients throughout the entire drug development lifecycle, from drug discovery to pre-clinical research and clinical trials.

Quality Assurance

Our Quality Assurance team focus on a broad range of roles across Good Manufacturing Practice (GMP), Good Clinical Practice (GCP) and Good Laboratory Practice (GLP).

Tech Ops and Engineering

Our experienced Technical Operations & Engineering recruitment team supports our clients across a range of areas including Supply Chain, Logistics and a range of Engineering roles.

Client Contact Form.

Complete the form and a member of i-Pharm’s Client Services department will contact you to discuss your specific need.