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
Nr. of Employees
small (1-50)
Pharmadvance
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.
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
Key Technologies
- Quality Management Systems (QMS)
- Pharmacovigilance system management (PSMF, ICSR, PSUR/RMP)
- Regulatory submission and dossier preparation
- Signal detection and risk management processes