About SYNRGY SCITECH
A pharmaceutical supply partner built on quality and documentation
We supply Active Pharmaceutical Ingredients, impurities, intermediates, and reference standards to pharmaceutical research, QC, and manufacturing teams worldwide.
SYNRGY SCITECH is a pharmaceutical supply organisation focused on Active Pharmaceutical Ingredients, impurities, intermediates, fine chemicals, and reference standards.
We were founded with a clear conviction — pharmaceutical raw materials, impurities and reference standards should be supplied with the same scientific rigour and documentation that the customer expects in their own laboratory. Our team works closely with formulation, R&D, analytical, and regulatory groups to identify, source and supply the materials they need to advance their research, validate their methods and remain compliant with evolving global expectations.
From our base in Mohali, Punjab (India), we serve pharmaceutical manufacturers, API producers, CROs, CDMOs, research institutions and quality laboratories. Each enquiry is reviewed by our scientific team and supported with documentation including Certificate of Analysis (COA), Material Safety Data Sheets (MSDS), and specification sheets, where applicable.
Across our published catalogue
From APIs to nitrosamine references
Pharmaceutical & research customers
Items shipped with COA where applicable
Mission
To enable scientifically sound pharmaceutical research and manufacturing by supplying high-quality APIs, impurities and reference standards with documentation, traceability and clarity.
Vision
To be a globally trusted documentation-led supply partner for pharmaceutical research, quality control, and analytical communities.
Values
Scientific integrity. Documentation discipline. Customer responsiveness. Long-term partnership over short-term transaction.
Quality-first sourcing, documentation-led supply
Our team brings together pharmaceutical sourcing, analytical, and regulatory experience to support the workflows that genuinely matter to our customers — method development, validation, impurity profiling, stability studies and ongoing release testing.
Read about our quality approachIndustries served
Pharmaceutical research, QC and manufacturing teams
Our customers operate at every stage of pharmaceutical development — from discovery research to commercial release.
Pharmaceutical manufacturers
Supporting commercial production teams.
API manufacturers
Reference materials for in-process control.
Formulation companies
Reference standards for assay and impurity testing.
CROs & CDMOs
Project-aligned supply with documentation.
QC / QA laboratories
Working and reference standards for routine release.
R&D laboratories
Method development and validation support materials.
Universities & research
Selected research-grade materials.
Regulatory & analytical teams
Genotoxic, nitrosamine and impurity standards.