Pharmassist ltd.

Pharmassist Ltd: Your Trusted Partner in Clinical Research

Pharmassist Ltd is a leading Contract Research Organisation (CRO) that has been providing high-quality services in clinical research, pharmacovigilance, regulatory affairs, medical affairs, and quality management since 1999. With offices located in Athens, Greece and London, United Kingdom, Pharmassist Ltd has established itself as a trusted partner for pharmaceutical companies looking to conduct clinical trials and bring new drugs to market.

At Pharmassist Ltd, we understand the importance of conducting clinical trials that are safe and effective. Our team of experienced professionals includes physicians, pharmacists, biostatisticians, data managers and project managers who work together to ensure that every trial is conducted with the highest level of quality. We have extensive experience working with both small biotech companies as well as large pharmaceutical corporations.

Our Services

Clinical Trials: We offer a full range of services for Phase I-IV clinical trials including study design and protocol development; site selection; patient recruitment; monitoring; data management; statistical analysis; medical writing; regulatory submissions and inspections.

Pharmacovigilance: Our team provides comprehensive safety monitoring services including adverse event reporting; signal detection activities; risk management plans development and implementation.

Regulatory Affairs: We provide support for all aspects of regulatory compliance including preparation of Investigational New Drug (IND) applications or Clinical Trial Authorisation (CTA) submissions to regulatory authorities such as the European Medicines Agency (EMA), Food & Drug Administration (FDA), or other national agencies worldwide.

Medical Affairs: Our team provides expert advice on medical issues related to drug development such as scientific communications planning or publication strategy development.

Quality Management: We offer comprehensive Quality Management System support including SOP development/revision/review/implementation/training/audit programs etc., GCP/GLP/GMP audits etc., CAPA management etc., vendor qualification/management programs etc..

Why Choose Pharmassist Ltd?

At Pharmassist Ltd we pride ourselves on our commitment to excellence. Our goal is always to exceed our clients' expectations by delivering high-quality results on time and within budget. Here are some reasons why you should choose us:

1. Experience - With over 20 years' experience in the industry we have developed an extensive network of contacts across Europe which enables us to deliver projects efficiently while maintaining high standards.

2. Expertise - Our team consists of highly qualified professionals with expertise across all areas required for successful drug development.

3. Flexibility - We understand that each client's needs are unique so we tailor our approach accordingly.

4. Quality - At Pharmassist Ltd quality is at the heart of everything we do.

5. Cost-effectiveness – As an independent CRO without any overheads from parent company ownerships or affiliations with other service providers like labs/CROs/etc., we can provide cost-effective solutions without compromising quality standards.

Conclusion

In conclusion, if you're looking for a reliable partner who can help you navigate through complex regulations while ensuring your clinical trial runs smoothly then look no further than Pharmassist Ltd! With our experienced team members who possess deep knowledge about various therapeutic areas along with their respective regulations/guidelines/policies/procedures/etc., coupled with state-of-the-art technology platforms/tools/software/hardware/etc.; there's no better choice than us when it comes down choosing someone trustworthy enough whom you can rely upon throughout your journey towards bringing new drugs into market successfully!