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Post-Marketing Surveillance

International and US companies rely on the expertise and professional resources of PDG to provide dependable, accurate, and compliant drug safety programmes, pharmacovigilance services, and ongoing assessments of labelling accuracy and completeness.

Drug safety programmes

International and US companies rely on the expertise and professional resources of PDG to provide dependable, accurate, and compliant drug safety programmes, pharmacovigilance services, and ongoing assessments of labelling accuracy and completeness.

An experienced post-marketing safety surveillance team

PDG’s array of epidemiologists, clinicians, statisticians, and regulatory experts deliver evidence-based analysis to address the safety and ongoing benefits / risk assessments of your drug products. The company’s services are predicated upon years of successful industry experience and regulatory interactions relating to both generic and brand name products.

Turnkey solutions for post-marketing surveillance of drugs

PDG provides turnkey solutions that include design and implementation of critical standard operating procedures, validation, training, quality control, and quality assurance. PDG safety surveillance activities may include:

  • Individual case reports
  • Safety database
  • Safety reports
  • Literature searches
  • Safety signal detection
  • Risk management initiatives

Clinical trial consulting and pharmaceutical consulting professionals will benefit by becoming current on adaptive trial design.
Safety surveillance and pharmacovigilance consulting to generic drug manufacturers, as well as generic drug labelling consulting may soon become a service in demand.
Pharmaceutical Development Group (PDG) is a drug and medical device consultant that continuously engages in meetings and interactions with the US Food and Drug Administration...
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