SeerPharma assists a multinational pharmaceutical company with on-site GMP validation activities.
SeerPharma sourced and deployed a contractor to assist with providing User Requirements Specifications (URS) and other validation documents for the company’s:
- Facilities and Heating, Ventilation and Air Conditioning (HVAC)
- Process Equipment
Documents were prepared in accordance with the company's standard SOPs and templates.
Our team of senior consultants also provided assistance with Computer System Validation (CSV).
SeerPharma’s Contracting arm of the business took away the headache of HR management and provided the client with easy access to qualified talent vetted by our Directors.
We have also supported validation activities in Active Pharmaceutical Ingredient (API) manufacturing.
Contact us if you require assistance with validation of facilities, equipment, processes or computer systems.
This post comes from our April 2016 Journal.
