Rajaswa Pharmaceuticals
RAJASWAPHARMACEUTICALS
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NABL TC-17877 · FDA approved · Pune

Precise testing.
Reports you can file.

Rajaswa Pharmaceuticals is an ISO/IEC 17025 accredited contract testing laboratory. We support pharmaceutical manufacturers with chemical and instrumental analysis, microbiology, method development and validation, computer system validation and reference standards.

Send a test enquiry Explore services
Integrity/Trust/Respect
Waters Acquity UPLC systemUPLC · Waters Acquity
Thermo Scientific UltiMate 3000 UHPLC systemsUHPLC · Thermo
Agilent GC-MS systemGC-MS · Agilent
ISO/IEC 17025:2017NABL · TC-17877 · valid to Apr 2030
FDA approvedForm 37 drugs · COS-23 cosmetics
WHO-GMP compliantCDSCO & State FDA inspected
ISO 9001 · 14001 · 45001Quality · Environment · Safety
21 CFR Part 11Compliant instruments & data
About Rajaswa

We help Indian pharmaceutical manufacturers with analytical testing, method development and method validation, and advise on non-clinical testing and regulatory submission preparation.

Quality first

Every result goes through independent review before the Certificate of Analysis is released.

Fair pricing

Competitive rates and rate contracts that make regular testing affordable.

Regulatory ready

Methods per ICH, USP, BP and IP, with data that stands up to audits.

Allopathic, Ayurvedic, cosmetics

Physical, chemical and instrumental testing across product types.

Analysts preparing samples at the bench
Our values

What every report stands on

Integrity

Every result is reported exactly as measured. Raw data, audit trails and reviews stay complete and traceable.

Trust

Accredited methods, calibrated instruments and on-time reports that customers and regulators can rely on.

Respect

For our clients' timelines and confidentiality, for our analysts, and for the patients who depend on safe medicines.

Services

Four service lines, one accredited lab

Ask about a test
15 SERVICES

Chemical & instrumentation

For all types of industries, from APIs and excipients to finished formulations and packaging.

  • Method development & validationICH Q2(R1) · USP <1225>
  • Method verification & transferUSP <1224> <1226>
  • Nitrosamines by GC-MS/MSTrace level
  • Elemental impuritiesUSP <233> · ICP-MS
Show all 15
  • Packaging material testingUSP <661.1> <661.2>
  • 5-batch analysis & batch release
  • API & excipient testingUSP · BP · IP
  • Residual solventsUSP <467>
  • Formulation development studies
  • Stability testingICH Q1
  • Dissolution studies
  • Forced degradation studies
  • Pharmacopoeial testing of materials
  • Cleaning / residue method development & validation
  • Complete water analysis
10 SERVICES

Microbiology

Microbial quality, sterility and validation work for products, water and environment.

  • Method development & validationMLT · BET · Sterility · PET
  • Microbial limit testMLT
  • Sterility test
  • Bacterial & depyrogenation endotoxinBET · DET
Show all 10
  • Cleaning validations
  • LBPC
  • Biological assay
  • Growth promotion testGPT
  • Water system validationPhase I · II · III
  • Environmental monitoring
5 SERVICES

Computer system validation

Validation and assurance for laboratory and GxP computerised systems.

  • Computer system validationGAMP 5
  • Computer software assurance verificationCSA
  • Challenge testing
  • Gap & risk assessments
  • Customer-specific requirements
4 SERVICES

Impurity & standard supply

Custom-made and ready-stock impurities and standards for QC and R&D.

  • Custom impurity manufacturing
  • Custom standard manufacturing
  • Quality systemISO 17025 · ISO 17034
  • Ready-stock impuritiesQuick dispatch
Instruments

Equipped for trace-level work

All instruments are regulated as per 21 CFR Part 11.

Mass spec

LC-MS/MS

Triple quadrupole · Agilent

Mass spec

GC-MS/MS

Triple quadrupole · Agilent

Elemental

ICP-MS

Thermo Scientific

Chromatography

UHPLC

Thermo Scientific UltiMate 3000

Chromatography

UPLC

Waters Acquity with PDA detector

Chromatography

HPLC

Waters Alliance 2695 with UV, PDA and RI detectors

Mass spec

GC-MS

Agilent 5973 MSD with HP 6890 GC

Chromatography

GC with headspace

PerkinElmer TurboMatrix & Agilent G1888, FID

Spectroscopy

FTIR

Bruker

Spectroscopy

UV-Vis

Agilent

Elemental

AAS

Thermo Scientific

Stability

Stability chambers

Thermolab · ACC, LT, INT & Zone IV

Stability

Photostability chamber

Thermolab

Physical

Dissolution

Labindia · Electrolab

Titration

Karl Fischer & autotitrator

Water content, potentiometry

Physical

Tablet testing

Disintegration, friability, hardness, viscosity

Analytical balancespH & conductivity metersMuffle furnaceLOD ovensPackaging material test set-up
Accreditation

Accredited and approved

Recognised by NABL, FDA Maharashtra (drugs and cosmetics) and IAF-accredited certification bodies.

NABLISO/IEC 17025:2017TC-17877 · valid to 12 Apr 2030
FDA MaharashtraForm 37 approvalMH/104445 · valid to 07 Mar 2027
FDA MaharashtraCosmetics testing approvalForm COS-23 · MH/104445 · valid to 15 Sep 2030
RICL · UAFISO 9001:2015Quality management · to Sep 2028
RICL · UAFISO 14001:2015Environmental management · to Sep 2028
RICL · UAFISO 45001:2018Occupational health & safety · to Sep 2028

MSME registered · UDYAM-MH-26-0471500. Scope of NABL accreditation can be verified at nabl-india.org.

Contact

Tell us what you need tested

Share the product, tests and specification. We reply with a quotation and turnaround time.

Emailsales@rajaswa.in
Phone+91 98817 40591
LaboratoryShop 01 & 02, Ground Floor, Trimurti Complex, Lavale Road, Lavale Phata (Opp. Datwyler), Pirangut, Tal. Mulshi, Pune, Maharashtra 412115
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