Freyr’s Scientific and Medical writing team has proven expertise in delivering world-class Regulatory and Medical Writing services for its growing clientele of (global large) Pharma, leading CROs and other Biotech companies adhering to stringent timelines and high-quality parameters. Freyr is a preferred global Medical Writing services provider for both writing and document level publishing requirements. Read More

Our compliance experts work closely together on local and international Regulatory and compliance challenges and offer specialized GxP audit, QMS Remediation, Process and Product Validation and GxP Solution consulting services to assist Life Sciences organizations comply with Health Authority requirements. Read More

Freyr understands Local Pharmacovigilance (PV) activities and provides end-to-end PV services such as Local QPPV ,National Person for Pharmacovigilance (NPPV ), Literature Monitoring, Signalling, Case Processing, ICSR, and setting up the entire Safety Database to meet the local requirements. Read More