For over 30 years SeerPharma has aided Pharmaceutical and Medical Device companies on matters of Quality Assurance and GMP compliance.
The current COVID-19 pandemic is seeing day to day quality related business operations challenged by attempting to deal with multiple personnel across different departments remotely. The need for immediate and continual collaboration is vital in ensuring quality activities are performed correctly, in a timely manner and GMP compliance is maintained.
In response to the current COVID-19 pandemic, SeerPharma is available to assist you virtually in real-time as required.
In the event you need an experienced resource to provide a quick sanity check on the document you are writing; or you require more detailed assistance reviewing supplier agreements; or a Validation Master Plan, SeerPharma is available to provide consulting/advisory assistance in a virtual environment to help you maintain business continuity.
Using platform technologies such as Zoom, Cisco Webex and Microsoft Teams and secure online sharing tools, SeerPharma is available to provide you real-time assistance with:
- General Quality Assurance and GMP compliance concerns
- Computer System Validation (including setting up a CSVMP and Infrastructure Qualification framework)
- Desktop auditing
- Reviewing Facility Designs for GMP Compliance
- Reviewing Supplier Agreements
- Virtual GMP training
