In vitro assays for drug registration in full compliance with ANVISA regulations. These include pharmaceutical equivalence studies, dissolution profiling, biowaiver studies, solubility assessments, dissolution dossiers and the development and validation of analytical methods.
We develop customized methodologies to meet specific needs in the pharmaceutical sector, whether for research and development or for quality control.
We support global expansion by partnering with international clients that require equivalence studies in Brazil, with a special focus on antineoplastic drugs.
Pharmaceutical equivalence ensures that generic and reference products contain the same active ingredient, at the same concentration, in the same dosage form and route of administration.
By adhering to rigorous quality standards, we guarantee that both products have identical qualitative and quantitative compositions and meet the same purity and potency requirements.
At Synvia, we combine over 20 years of experience in the pharmaceutical sector with a highly qualified team to deliver solutions that make a difference.
pharmaceutical industry clients served in Brazil and around the world
multidisciplinary professionals, including dozens of master’s and PhD holders with high-level technical and scientific expertise
of proprietary and specialized infrastructure
and an unwavering commitment to quality and precision
Modern facilities equipped with cutting-edge technology, including:
Area specialized in the evaluation and optimization of resources, deadlines, and investments to ensure each project achieves its full potential.
Area responsible for real-time monitoring, ensuring full visibility and strict compliance with agreed deadlines.
Experts in the efficient importation of standards and raw materials essential for analytical processes.
A dedicated area for producing detailed analyses and precise reports, ensuring clarity and reliability in the presented results.
A comprehensive system aligned with the highest technical and regulatory standards, to guarantee total quality across all stages.
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