GMP Specialist

Dorota Osińska is a Pharmacist with over the 20 years experience in pharmaceutical industry. She worked in the research department of a pharmaceutical company developing and implementing oral pharmaceutical forms. She has been a lead expert in validation and audits in Quality Assurance and Quality Assurance and Qualified Operations Manager at Polfa Warszawa S.A. (Polpharma Group) as well as the Manager of Compliance and Quality Assurance Compliance Team at Agila Specialties Polska (Mylan Group).

She participated in designing and launching new production areas and upgrading existing ones. As a quality specialist, she participated in the implementation of Good Manufacturing Practice requirements. She was an internal auditor and external auditor, auditing the manufacturers of active substances, packaging materials, medical devices, contract manufacturers and pharmacovigilance.

She oversaw the development of quality contracts, development of DGMW, complaint handling, qualitative documentation management, deviation analysis, supplier qualification, corrective and preventive actions, internal training, internal inspections and external audits.

Ms Dorota Osińska has started GMP certification process in the field of labelling, re-labelling and re-packing of investigational products.

Go back

News

Completion of a single-center phase I study of the safety and pharmacokinetics of CPL207280

We have just completed a phase I study of safety and pharmacokinetics (part B) of an innovative therapy that could be used...

Read more …

GcLP quality certificate for laboratory procedures

The BRG Clinical Site received the GcLP quality certificate for laboratory procedures and is in the process of obtaining GMP certification for pharmaceutical procedures.

Read more …

Study for healthy people with a drug against Covid-19

In BRG we are currently performing a study for healthy people with a drug against Covid-19 .
In the project we are comparing experimental injectable drug called...

Read more …

Phase I study finished

Our site has just succesfully finished clinical stage of phase I (two parts) study with JAK kinase inhibitors.

Read more …

Safety and Pharmacokinetics of JAK/ROCK Inhibitor in Healthy Volunteers

In BRG we are just starting Study for Healthy People with an Immune Drug - Part B. The aim of the following clinical trial...

Read more …

About Us | Services | Our Site | Partners | Smoking Risk Study | Contact Us

Early Phase Clinical Trials

2024 © Bio Research Group. All rights reserved.

 

scroll to top ▲