Facility

Collaborate to Innovate

ASBL, a contract research organization (CRO), works in state-of-the-art pre-clinical and bioanalytical facilities to empower our mission to serve the human and animal health care companies by constant improvement in its capabilities and capacities to conduct high-quality research. ASBL believes in the constant upgradation of personnel, facilities, and equipment which makes ASBL as an energy-efficient and cost-competitive research organization.
We would like to invite our prospective clients to visit the ASBL facilities and to meet our scientific team. To schedule a visit, you can contact us through mail (bd@asblifesciences.com) or call us at +91 888-650-8833.

  • Quality Systems 

         - Maintenance of optimal environmental conditions for housing of animals as per CPCSEA
         - Procurement of animals from certified vendors
         - Periodic animal health monitoring
         - Feed, water and Bedding material analysis as per SOP
         - Ethical efforts to avoid pain and distress to animals subjected to experimentation as well as 
           use of Anesthesia and Euthanasia as per CPCSEA guidelines 
         - Bio-waste disposal as per recommendations of State Pollution Control Board   
         - Appropriate measures instituted to ensure safety of personnel working in animal facility

  • Certifications and Compliances

         - Registered with CPCSEA and constituted IAEC 
         - Institutional Bio Safety Committee (IBSC) registered under DBT 
         - EMS (Environment Management System  as per ISO 14001) 
         - QMS (Quality Management System) as per ISO 9001:2008

  • State-of-art GLP complaint Bioanalytical/ Analytical facility equipped with high-end instrumentation such as Mass Spectrometers, Gas and Liquid Chromatographs. 
  • Quantitative bio-analysis of active drugs, natural compounds and metabolites in biological fluids such as plasma, serum, whole blood, urine
  • Experienced in developing Bioanalytical assays for NCEs and large molecules like peptides and proteins
  • Expertise in developing and validating Bio-analytical method for Complex molecules, Chiral molecules, Derivatization techniques, Conjugates and Un-conjugates
  • Method Development: as per Quality by Design (QbD) and latest regulatory requirements.
  • Method Validation: As per ICH, USP/USFDA, ANVISA, MCC and TGA requirements or as per customer defined protocol
  • Part-11 Compliance Software
  • Experience of more than 1000 Bioequivalence studies for various regulatory submissions i.e. (USFDA, UK, EU, ANVISA, MoH Turkey, TGA, WHO and Canada etc)

WE DELIVER SCIENCE USING BIOLOGY

Every Client admires our Deliverables