Specialized in the Synthesis of Pharmaceutical Impurity Reference Standards, API Impurities
Specialized in the Synthesis of Pharmaceutical Impurity Reference Standards, API Impurities and execution of pharmaceutical development and product launch
GlobeSynth Pharma Tech have 4000+ API impurities, Standards, Intermediates In-Stock with us which is more than 95% purity/potency.
We pledge to use ICH-GMP/GLP procedures in our manufacturing process for the benefit of our esteemed clients, and we aspire to provide high-quality services.
GLOBESYNTH PHARMA TECH, an ISO-certified Contract Research Organization (CRO), started in 2018, has its own manufacturing facility in Salem, Tamil Nadu, India.
GLOBESYNTH PHARMA TECH is specialized in the Synthesis of API Impurities, Process Impurities, Degradation Impurities, Potential Impurities, Building Blocks, metabolites of active ingredients and excipients, Medicinal Discovery Chemistry, Custom Synthesis, Materials Chemistry, Library Design and Synthesis, Chiral Synthesis, Peptide Synthesis, Nucleic Acids Chemistry and Process Chemistry. We are a group of highly skilled chemists with backgrounds in higher education who provide a variety of customized synthesis services to the pharmaceutical, agricultural biotechnology and veterinary industries.
Our Vision
To become leading global Impurity Reference Standard Company and one among the top 10 by 2022" and mainly focus on sustainable and profitable growth to achieve our target customers are, India, US and Europe based markets
Our Mission
Our main mission to help our clients will be the Active Pharmaceutical ingredients manufacturers who are willing to procure reference standards and intermediates which is either pharmacopeia or non-pharmacopeia with high quality standards of Data carrying Certificate of Analysis as per Standards.
Our Values
Honesty, integrity and transparency Innovate everywhere Creativity driven by diversity Uncompromising quality Committed to our customers Customers confidentiality will be maintain strictly
