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Medicinal products
Investigational Medicinal Product (IMP)
Cell & gene therapy (ATMP)
Medical devices
Veterinary products
Food suplements
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Why should you work with us?
Our teams
Contact
Product Development
Development
Regulatory Due Diligence
Project management
Preclinical and clinical development
Commercialization
Market Analysis
Support and brokerage in product portfolio optimization
Clinical Trials
Study set-up
Paediatric Investigation Plan
Study conduct
CSR writing / preparation
Full service Clinical Research Organization
PhV in Clinical Trials
Quality
CMC development
Nitrosamines
Risk assessment and Control of Elemental Impurities
Stability Study Design
Impurities & Genotoxicity
Technology and analytical methods
Analytical Methods Transfer
GMP system
GMP system implementation
Product certification
GxP Audits
GMP
GMP Audits (remote and on site)
Audit of manufacturing sites/ laboratory
Support in preparation to inspection
GCP
GCP Audits (remote and on site)
PhV
GVP Audits (remote and on site)
GLP
GLP Audits (remote and on site)
Regulatory Affairs
Pre-authorisation
Regulatory Roadmap
Scientific Advice
Product information
Preparation of product information
Package Leaflet readability test
Bridging Report
Translation of Patient Information
Product Information and mock-ups verification
Dossier preparation
Medical writing - preparation of registration dossier
CTD Module 3 - Quality
Application Form preparation
Product information
Enviromental Risk Assessment (ERA)
Orphan Medicinal products
Preparation of the clinical part
Dossier Gap Analysis
MA Handling
Handling of the registration process
eCTD compilation
Post-authorisation
Post-authorisation procedures support
Product lifecycle management
Medical Information
Sunset clause
OTC switch
Transfer of MA
Promotional materials review
Regulatory outsourcing
Regulatory consulting in the pharmaceutical industry
MAH service
Pharmacovigilance
PhV system
Pharmacovigilance system (PSMF)
xEVMPD management
RMP Development and maintenance
Regulatory Intelligence
PhV post-authorisation
Addendum to Clinical Overview Development
Local literature monitoring
Local Contact Person for Pharmacovigilance
ICSR management
PSUR preparation
Clinical trials
EU QPPV service
QP Service / Importer
QP Service
Import and supply chain management
MIA Licence
GMP Certificate
Importer Warehouse
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