Pharmaceutical Analysis Testing Services
Pharmaceutical Analysis Testing Services

Pharmaceutical Analysis Testing Services

Price 199 INR/ Piece

MOQ : 1 , , Piece
 

Pharmaceutical Analysis Testing Services Trade Information

  • Minimum Order Quantity
  • 1 , , Piece
  • FOB Port
  • Ahmedabad
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID)
  • Delivery Time
  • 7 Days
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Packaging Details
  • ANY
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • ISO
 

About Pharmaceutical Analysis Testing Services

Akshar Analytical Laboratory & Research Center is deeply committed to offering superiorPharmaceutical Analysis Testing Servicesin order to satisfy the many needs of our valued customers. Our professionals oversee the performance of this service, ensuring that it meets all quality requirements set out by prominent industries. Our highly skilled personnel employ the greatest equipment and cutting edge technologies to provide this service. Additionally, the provided service is extremely dependable and executed in accordance with the established quality standards...



Comprehensive Testing and Standard Compliance

We ensure pharmaceutical products are tested in full alignment with globally recognized standards such as IP, BP, USP, and EP. Our services encompass key parametersassay, dissolution, impurity profiling, stability, and microbiologyto deliver reliable quality assessment across multiple sample types.


Advanced Analytical Techniques and Accreditation

Utilizing state-of-the-art equipment and methodologies (HPLC, GC, UV, IR, TLC, KF, and AAS), our laboratory upholds ISO/IEC 17025 certification. This accreditation assures precise, reproducible results for all product evaluations, reinforcing confidence in your data and regulatory submissions.


Efficient Turnaround and Confidential Reporting

Reports, including comprehensive analytics and COA, are typically issued within 715 days. We enforce strict client data confidentiality protocols, so your proprietary information remains protected at every stage. Our service includes tailored reporting to facilitate regulatory approvals globally.

FAQs of Pharmaceutical Analysis Testing Services:


Q: How do you ensure compliance with pharmaceutical testing standards like IP, BP, USP, and EP?

A: Our laboratory strictly follows established protocols for each standardIndian Pharmacopoeia (IP), British Pharmacopoeia (BP), United States Pharmacopeia (USP), and European Pharmacopoeia (EP). Trained analysts and validated methods ensure each test meets regulatory specifications, providing results accepted globally.

Q: What parameters can Pharmaceutical Analysis Testing Services analyze for my product?

A: We routinely conduct assay, dissolution, impurity profiling, stability studies, and microbiological assessments. Using advanced instrumentation, we deliver thorough evaluations for tablets, capsules, syrups, injections, and bulk drugs.

Q: When can I expect to receive the final analytical report and Certificate of Analysis (COA)?

A: Our standard turnaround time is 715 days upon receiving your sample. Reports are comprehensive and include all analytical data as well as a Certificate of Analysis, expediting regulatory submission or internal review.

Q: Where are the Pharmaceutical Analysis Testing Services conducted and which sample types are accepted?

A: Testing is performed at our ISO/IEC 17025 accredited facility in India. We accept a wide variety of sample matrices, including tablets, capsules, syrups, injections, and bulk pharmaceutical ingredients.

Q: How is client data confidentiality maintained throughout the testing process?

A: We implement strict data protection measures, ensuring that all client information, test results, and proprietary details remain secure. Only authorized personnel handle your samples and analytical data.

Q: What analytical techniques do you employ and what benefits do they offer?

A: Our facility utilizes HPLC, GC, UV, IR, TLC, KF, and AAS, which enable us to deliver reliable, accurate, and sensitive assessments for diverse pharmaceutical products. These technologies support robust quality control and regulatory compliance.

Q: Do you provide assistance with regulatory documentation for DCGI or USFDA submissions?

A: Yes, our service includes comprehensive documentation support for regulatory submissions to DCGI, USFDA, and other authorities. We structure reports and analytical data to meet the requirements of global regulators, enhancing smooth approval processes.

Tell us about your requirement
product

Price:

Quantity
Select Unit

  • 50
  • 100
  • 200
  • 250
  • 500
  • 1000+
Additional detail
Mobile number

Email

More Products in Pharmaceutical Testing Services Category

Total Alkaloids Testing Services

Total Alkaloids Testing Services

Price 199 INR / Piece

Minimum Order Quantity : 1 Piece

Ayurvedic Cough Syrup Testing Services

Ayurvedic Cough Syrup Testing Services

Price 199 INR / Piece

Minimum Order Quantity : 1 Piece

Food Contact Migration Testing Services

Food Contact Migration Testing Services

Price 199 INR / Piece

Minimum Order Quantity : 1 Piece

Surgical Products Testing Services

Surgical Products Testing Services

Price 199 INR / Piece

Minimum Order Quantity : 1 , , Piece



Back to top