We offer the following cGMP compliant services for Drugs and Pharma:

Analytical Method Developments and Validations
  • Stability Storage and Analysis
  • Pharmacopeial Testing
  • Elemental Impurity Analysis by ICPMS( Screening, Validation, Batch Analysis)
  • Raw Materials and Excipients Analysis
  • Comparator Testing (Dissolution Profile)
  • De Formulation Studies (Reverse Engineering)
  • Extractables and Leachables
  • Carryover studies
  • Force Degradation Studies
  • Impurity Isolations and Identification
  • Genotoxic Impurity Studies
  • Drug/Excipient Interaction Studies
  • Physico - Chemical Analytical Studies
  • Ion Chromatography
  • Polymorphism (pXRD)
  • Particle Size Determination (PSD) services
  • Binding Studies
  • NMR Services


Microbiology Division at Perfomics undertakes analysis for Industries associated with Drugs, Cosmetics, Disinfectants and water as per IP/BP/EP/USP-NF/WHO methods. Our lab provides the following services:

  • Total Microbial Count
  • Detection of Pathogens
  • Sterility Testing
  • Water Analysis
  • Method Validations
  • Microbiological Assay of Antibiotics


We provide high-quality BA/BE services that are personalized to meet Client's specific application. We offer the following tasks to our clients:

Method Development, Method Validation (MD/MV) and analysis of samples for clinical trials

  • BA/BE studies
  • Pharmacokinetic (PK) studies
  • Drug-Drug interaction studies
  • NCE Bio Analysis
  • We offer clinical services in association with various Indian CRO's
  • Phase I to IV studies Measure drugs and metabolites in the biological matrix ( Whole Blood, Plasma, Serum & Urine) of samples from pre-clinical and clinical studies
  • Specialized to develop highly sensitive assays for Small Molecules, Peptides and Proteins
  • Cost Effective services with minimum turn-around time


Our team of experienced scientists specializes in creating alternate and patentable processes for various novel formulations. Our state-of the art development facility is equipped to carry out various processes such as API Characterization, Pre-Formulation Studies, Excipient Compatibility Studies, Composition and Process Optimization, Stability Studies in line with ICH And WHO, Scale-Up And Process Validation and Manufacture of Registration/ Submission Batches to meet stringent norms of regulatory bodies. We develop formulations in conventional dosage forms of Solid & Liquid orals, Topical Preparations and Powders & Granules for reconstitution. We are also capable of developing products of specialized dosage forms targeted for special release patterns (extended / delayed), solubility (dispersible / soluble), taste optimization, floating tablets and pH sensitive drug deliveries.


Test systems
Rats, Mice, Guinea Pigs, Rabbits and Hamsters
Routes of administration
Intravenous, Oral, Topical, Subcutaneous, Intramuscular, Dermal and Intraperitonealetc..
Pharmacokinetic trials
In all the test systems mentioned above
Toxicity studies / Toxicokinetictrials
In-vivo studies: Acute, Sub-acute, Chronic studies, male and female fertility, teratogenicity tests, developmental toxicity tests, chronic and combined carcinogenicity tests
In-vitro studies: LAL test for endo-toxin assay, skin irritation test, Genotoxicity and Mutagenicity tests, Hair follicle stimulating Assay etc..

Bio-assays and other tests (Various Pharmacopeia Guidelines)
In Rats, Mice, Guinea Pigs and Rabbits
Special services
Anti-sera production (Antibody production), Blood, Plasma and Serum services
Whole blood perfusion, Jugular vein cannulation
Biocompatibility trials •Laboratory services
Histopathology services, Immunization trials, Clinical pathology services, Analysis and reporting
Archiving services…
Tissue specimen, Histopathology or blood smear slides and documents

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