Regulatory
Affairs

Regulatory affairs is a profession developed from the desire to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare.

Pharmacovigilance
Services

With a team of PV experts including experienced PV physicians, medics and access to our medical writing group, we offer a fully compliant and high-quality complete package of PV services.

Our goal is to help our customers ensure regulatory compliance, along with managing the risk-benefit profile of their products, in order to maximise product potential and ensure patient safety.

Services We Provide

Submission and Publishing
Artwork and Labelling
Regulatory Intelligence
Medical Writing
Market Access & Commercial
End-to-End Support

At Pharmazone

We offer

Global Life Science Submissions

We handle global life science submissions' pre-market and post-market activities.

Regulatory Intelligence Expertise

We translate regulatory requirements into practical, workable plans.

Compliant Regulatory Dossier Services

We ensure dossier compliance with CGMP, ICH, GCP, GLP guidelines.

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Global Clients
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Project Executed Globally
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Affiliate Partners
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Global Affiliate Network
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Supported Products Globally