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The Benefits of outsourcing Pharmacovigilance to PDS

Outsourcing PV (pharmacovigilance) is becoming an increasingly viable option for many life sciences and healthcare companies of all sizes. Whilst employing full-time staff is still common, more and more companies are realising there are significant benefits to outsourcing some, or even all aspects of pharmacovigilance to a specialist provider such as PDS.

The key benefits

There are many key benefits to outsourcing pharmacovigilance to PDS including, but not exclusively:

  • Dedicated specialists in Pharmacovigilance
  • Dedicated professional staff, trained to the most current PV standards and regulations
  • Reduced operating costs e.g., no recruitment, training, pension, sickness or holidays to pay for
  • Flexibility of resources – only pay for PV resources when you need them
  • Diversity and broader depth of PV expertise and experience
  • Maintain an objective, professional view of your quality compliance, e.g., independent review of your SOPs, documentation and processes.
  • A dedicated, validated and cost effective PV Data Base
  • Reduced technology costs – no licences, validation, support or training fees.

Working with PDS means you have a highly trusted partner who adds value to your business through quality of service, remaining up to date with the latest regulations (such as ISO IDMP) and staff training, whilst providing an objective insight to your business’s compliance status.

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Pharmacovigilance

Pharmacovigilance

Using our experience and knowledge to guide you through the complexities of Pharmacovigilance. We have over 60 years’ experience working alongside national and international Pharmaceutical and Biotech companies.

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EVMPD and XEVMPD

EVMPD and XEVMPD

With an increasingly competitive market place and new initiatives like EVMPD and xEVMPD, the need for outsourcing specialist activities is of benefit to pharma companies.

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ISO IDMP

ISO IDMP

The implementation of IDMP is arguably the most significant development in drug safety, since the inception of systematic safety reporting back in the 1960’s.

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Regulatory

Regulatory

A bespoke service giving you comprehensive solutions in a proactive framework.

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Medical writing

Medical writing

We offer you our significant experience and expertise in professional medical writing, not only across a wide range of therapeutic areas but also in preparing quality documents for all stages of drug/product development.

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Patient information

Patient information

We offer you our wealth of experience in creating and delivering Patient Information User Testing.

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