Integrity
Every result is reported exactly as measured. Raw data, audit trails and reviews stay complete and traceable.
NABL accredited pharmaceutical testing lab · Pune
Precise testing.
Precise testing.
Reports you can file.
Rajaswa Pharmaceuticals is a NABL accredited (ISO/IEC 17025) and FDA approved contract testing laboratory in Pune. We support pharmaceutical and cosmetic manufacturers across India with HPLC, LC-MS and GC-MS analysis, microbiology testing, analytical method validation, computer system validation and reference standards.
Integrity/Trust/Respect
UPLC · Waters Acquity
UHPLC · Thermo
GC-MS · AgilentHPLC-01 · Assay & related substancesAcquiring
Sample RP/26-0412Run 00:00Signal 0.0 mAU● SST passed
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
A pharmaceutical testing laboratory in Pune that helps manufacturers across India with analytical testing, method development and method validation, and advises 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.
Our values
What every report stands on
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
Ask about a test
Pharmaceutical testing services from one NABL accredited lab
15 SERVICES
Chemical & instrumentation
For all types of industries, from APIs and excipients to finished formulations and packaging.
- Method development & validation
ICH Q2(R1) · USP <1225> - Method verification & transfer
USP <1224> <1226> - Nitrosamines by GC-MS/MS
Trace level - Elemental impurities
USP <233> · ICP-MS
Show all 15
- Packaging material testing
USP <661.1> <661.2> - 5-batch analysis & batch release
- API & excipient testing
USP · BP · IP - Residual solvents
USP <467> - Formulation development studies
- Stability testing
ICH 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 & validation
MLT · BET · Sterility · PET - Microbial limit test
MLT - Sterility test
- Bacterial & depyrogenation endotoxin
BET · DET
Show all 10
- Cleaning validations
- LBPC
- Biological assay
- Growth promotion test
GPT - Water system validation
Phase I · II · III - Environmental monitoring
5 SERVICES
Computer system validation
Validation and assurance for laboratory and GxP computerised systems.
- Computer system validation
GAMP 5 - Computer software assurance verification
CSA - 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 system
ISO 17025 · ISO 17034 - Ready-stock impurities
Quick dispatch
Instruments
HPLC, LC-MS and GC-MS testing at trace level
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
NABL accredited and FDA approved testing laboratory
Recognised by NABL, FDA Maharashtra (drugs and cosmetics) and IAF-accredited certification bodies.
MSME registered · UDYAM-MH-26-0471500. Scope of NABL accreditation can be verified at nabl-india.org.
Gallery
Standard instruments in our lab
Instruments in the Rajaswa laboratory. Click any instrument to view it larger.
Knowledge centre
From the Rajaswa lab
Short, practical notes on pharmaceutical testing, cosmetic testing, method validation and regulatory requirements. A new article every week.
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FAQ
Questions about our testing laboratory
Is Rajaswa a NABL accredited testing laboratory?
Yes. Rajaswa Pharmaceuticals is accredited by NABL to ISO/IEC 17025:2017 in the field of testing (certificate TC-17877, valid until April 2030). The laboratory is also approved by FDA Maharashtra under Form 37 for drugs and COS-23 for cosmetics.
Where is the laboratory located?
The laboratory is at Lavale Phata, Pirangut, Pune, Maharashtra 412115. We accept samples from pharmaceutical and cosmetic manufacturers across India by courier or hand delivery.
Which tests do you perform?
Assay, related substances and impurities by HPLC and UPLC, LC-MS and GC-MS work including nitrosamines, residual solvents by headspace GC (USP <467>), elemental impurities, dissolution, stability studies, water and packaging material testing, and microbiology such as MLT, sterility, BET and environmental monitoring.
Do you test cosmetics and Ayurvedic products?
Yes. We hold FDA Maharashtra COS-23 approval for testing cosmetics and their raw materials, and our ISO scope covers allopathic, Ayurvedic and cosmetic products.
Do you provide analytical method validation?
Yes. We develop, validate, verify and transfer analytical methods as per ICH Q2, USP <1225>, <1224> and <1226>, including cleaning method validation and forced degradation studies.
What is the turnaround time?
Our standard turnaround time is 7 days from sample receipt. Send your specification and test list and we will confirm the timeline and quotation.
Careers
Build your career in pharmaceutical testing
We are always looking for careful, curious people who want to work on modern instruments in an accredited laboratory. Send us your resume and we will contact you when a suitable position opens.
QC
QC Chemist / AnalystHPLC, UPLC, GC, wet chemistry · M.Sc. / B.Pharm / M.Pharm
MB
MicrobiologistMLT, sterility, BET, environmental monitoring · M.Sc. Microbiology
QA
Quality AssuranceDocumentation, data review, ISO/IEC 17025 systems
TR
Trainee / FresherRecent graduates keen to learn GLP laboratory practice
Thank you, your resume has been received.
Our team will review it and contact you if your profile matches an opening.
Our team will review it and contact you if your profile matches an opening.
Contact
Tell us what you need tested
Share the product, tests and specification. We reply with a quotation and turnaround time.
Existing customer? Track your sample status and download COAs online.Customer Login →
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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