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ARSI Canada Inc vs Sai Life Sciences

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CategoryARSI Canada IncSai Life Sciences
Listed sitebothcdmo
SummaryARSI Canada is a specialized CRO offering custom synthesis, API scale-up, analytical method development, and drug development services with over 50 years of combined experience and a GMP manufacturing facility in Bangladesh.Integrated CRDMO offering discovery, development, and manufacturing services for small molecule NCE programs across 280+ global pharma and biotech clients.
Services
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
  • CMC Analytical Development
  • Analytical Method Development & Validation
  • Process Development
  • Technology Transfer
  • Stability Testing & Storage
  • Quality Control Testing
  • CMC Regulatory Submission Support
  • CMC Analytical Development
  • Process Development
  • Stability Testing & Storage
  • Technology Transfer
  • API Synthesis & Manufacturing
  • Small Molecule Development & Manufacturing
  • ADC (Antibody-Drug Conjugate) Manufacturing
  • ADC Payload & Linker Synthesis
  • Flow Chemistry & Continuous Manufacturing
  • CMC Regulatory Submission Support
  • Solid-State Chemistry & Polymorph Screening
  • Formulation Development
  • Quality Control Testing
Modalities
  • Small Molecule
  • Small Molecule
  • Antibody-Drug Conjugate (ADC)
IndicationsData not yet provided.Data not yet provided.
Locations
  • Headquarters & R&D, Mississauga, Ontario, Canada
  • GMP Manufacturing, Bangladesh, Bangladesh
  • Headquarters, India, India
  • UK Office, UK, United Kingdom
  • USA Office, USA, United States
  • Boston Laboratory, Boston, Massachusetts, USA
  • Headquarters, Hyderabad, Telangana, India
  • Bidar Campus (Unit IV & VI), Bidar, Karnataka, India
  • Boston, Boston, Massachusetts, USA
  • UK Facility, United Kingdom
  • UK Operations, United Kingdom
  • Bidar Campus (API Manufacturing), Bidar, Karnataka, India
  • Integrated R&D Campus, Hyderabad, Telangana, India
  • Boston Area Site, Boston, Massachusetts, USA
CertificationsData not yet provided.
  • USFDA · Identifier: 21 CFR Part 210 and 211
  • EU · Identifier: EU cGMP guidelines
  • TGA · Identifier: TGA guidelines
  • India · Identifier: Schedule M (Indian cGMP standards)
  • My Green Lab (MGL) · Identifier: Green Lab Certification (98%+ compliance score)
  • BSE · Identifier: 544306
  • NSE · Identifier: SAILIFE
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.