At Panacea we believe in a better way of doing things. Everyone talks about delivering a fresh, dynamic, approach – but at Panacea you will find that we deliver on this promise. Our highly experienced team enjoy working with clients to find the best way to safeguard their investment and reputation, and we take pride in providing the best possible vigilance and regulatory affairs services to the pharmaceutical industry. Currently, Panacea are responsible for Marketing Authorisation’s in every EU country and have an international reputation which is respected by regulators.
What we do…
We provide outsourced pharmacovigilance and related services to companies at the clinical trial, Marketing Authorisation application, and the post authorisation phases. Our team also has expertise in:
- Medical Device Vigilance
- Veterinary Vigilance
- Quality Management & Auditing
Whether it’s a licence application, extension or variation, our regulatory affairs experts have the experience to ensure that your applications are built, submitted and approved to the highest standard of quality. Combined with our pharmacovigilance services, we have the ability to expand and safeguard your product portfolio.
How we do it…
We are flexible and responsive, whether it’s a one-off task, a fixed term project (large or small) or a continuous relationship over several years. We know that each client is different; each has a specific budget, timescale, and objective, and we do everything we can to work with them to ensure that budget targets are met, timescales respected, and objectives achieved. Individually, everyone at Panacea takes personal responsibility for providing the highest quality of work. Collectively, we offer a responsive, cost effective, flexible, and professional service.
Click on the video to find out more about the Panacea team.