Analysis of raw material:
Evaluation of raw materials and verification of specifications. Supplier Validation. Comparative analysis between raw materials.
Analysis of products in the market:
Product monitoring in the market, evaluation of products from the competition, physicalchemical and microbiological characteristics analysis.
Search and analysis of the bibliographic information about the product group. Models and variants, raw materials, certificates, sales prices, consumption data and contact of reference health professionals.
Obtaining clinical data and analyzing, evaluating and writing Clinical Evaluation reports. Bioequivalence of medical device and clinical justification of the project.
Certification of Raw Material:
Execution of tests under specific regulations, drafting of the technical dossier to obtain a specific raw material grade.
Tests on bioequivalent products to know their physicochemical characteristics and suitability for use. Advice on critical specifications.
R&D “a la carte”:
Planning product development projects. Advice and process engineering.
Tests under the European Pharmacopoeia:
Design of the dossier of trials for new drugs, development of new products based on bioequivalence.
Definition of the grades of raw material required for a new farmsanitary development.