Pharmadvance


Pharmadvance is a pharmaceutical consulting company dedicated to providing expert services in Regulatory Affairs, Quality Assurance, Entity Licensing, and Marketing and Advertising of medicines and healthcare products. They aim to support and grow with their clients by offering tailored solutions in the pharmaceutical sector.

Industries

Consulting
Pharmaceutical
Wholesale
Pharmaceutical Manufacturing

Nr. of Employees

small (1-50)

Pharmadvance


Products

Wholesale Distributors

Licensing services for wholesale distributors of medicinal products for human and veterinary use.

Wholesale Distributors of Medical Devices

Licensing services for wholesale distributors of medical devices.

Pharmacovigilance

Comprehensive pharmacovigilance consulting services including PSMF setup, ICSR management, literature monitoring, and audit support.

Licenciamento de Entidades

Apoio a empresas que pretendem licenciar a atividade de fabrico ou distribuição por grosso de medicamentos e dispositivos médicos.

Assuntos Regulamentares

Serviços de consultoria em assuntos regulamentares para medicamentos e produtos de saúde.

Manufacturers of Medicinal Products for Human and Veterinary Use

Licensing and regulatory consulting services for manufacturers of medicinal products for human and veterinary use.

View All Products

Services

Consulting for regulatory activities across product lifecycles for medicines, medical devices, cosmetics and supplements.

Implementation and maintenance of QMS, internal and mock audits, change control, deviation management, CAPA and risk management.

Support for licensing manufacturing and wholesale distribution activities and ensuring compliance with Good Practices.

Regulatory review, preparation and notification of advertising materials, product marketing support and market research.

Comprehensive pharmacovigilance services including PSMF, SOPs, literature monitoring, ICSR management, PSUR/RMP preparation, signal detection, training and local QPPV services.

Training, technical and scientific translations, and legal/regulatory support related to healthcare products.

Expertise Areas

  • Regulatory affairs and lifecycle management
  • Quality assurance and QMS implementation
  • Entity licensing for manufacturing and distribution
  • Pharmacovigilance and drug safety management
  • Show More (3)

Key Technologies

  • Quality Management Systems (QMS)
  • Pharmacovigilance system management (PSMF, ICSR, PSUR/RMP)
  • Regulatory submission and dossier preparation
  • Signal detection and risk management processes
  • Show More (1)

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