Skip to content Skip to footer
Lab
About us

Our Purpose

Paean Laboratories Private Limited is cGMP/cGLP contract testing laboratory located in Bangalore, INDIA. We provide Analytical and Microbial testing solutions to the pharmaceutical industry. We have a state of the art facilities with a built up area of 21,000 sq.ft. At Paean labs, our team consists of highly qualified professionals in the filed of chemistry, pharmacology, Microbiology, Quality assurance and quality control, they ensure that every analysis is conducted with utmost precision and adhering to regulations.

0 +
Years
0 +
Divisions
0 +
Countries
0 +
Employees

Advancing medicine,

innovating to improve lives

Icon

Vision

To excel as one of the most trusted partners cum consultant to our esteemed clients in providing highest standards of services in the field of analytics, micro testing and Quality Assurance in providing end to end solution for market leaders in the pharmaceutical, healthcare and food industries.
Icon

Mission

To reach beyond our customers’ expectations with innovative and bespoken services in the domains of analytics, microbiology testing, assurance, and certification for their global operations specifically for the pharmaceutical, healthcare and food industries with fast track and cost effective approaches that would be second to none.
Icon

Values

We stand for an integrated service package through highest order honesty, integrity, and responsibility with an uncompromising commitment to Quality and Customer service.We intend to create and evolve a customer friendly working atmosphere in a participatory mode.We possess a specific set of well qualified , like minded professionals who always display excellence in their respective fields under an inbuilt bondage of mutual trust and belief.
About us

Our Capabilities

Nitrasamines, NDSRI’s and Genotoxic impurities:

Evaluation, development and validation ofanalytical procedures as per USFDA, EMA and ICH guidelines.

Extractable and Leachable testing:

Extractable and Leachable studies for pharmaceutical industry ondrug delivery devices, container closure systems and its finished product.

Particle size distribution (PSD):

Development, validation of Particle size distribution methods (lightobscuration method) by using Malvern 3000.

Potentiometric testing:

Validation/verification of Potentiometric assays by using aqueous electrode, Non aqueous electrode, Silver ring electrode, Complexometric titrations using copper AgCl electrode - copper reference electrode, Optrode etc.

Method development and Validation:

Analytical method development and validation for Assay, Related substances, residual solvents, dissolution etc.
Dissolution studies: Method development and Validation of dissolution tests, as per USP/BP/EP/IP for oral solids and suspensions.

Elemental Analysis:

Method development and validation of analytical methods by ICP-MS as per USP<232> and USP <233> for oral solids, Parenteral and Inhalation products.

Residual solvents:

Evaluation of residual solvents and purity of Nitrogen gas by GC-HSS Using Flameionization detectors (FID) and TCD (Thermal conductivity detector (TCD)
Testing of Raw material, Excipient and Finished product testing.

Stability Studies:

Stability studies as per ICH guidelines.
Evaluation of pesticides as per USEPA guidelines.
Evaluation of Phthalates by using GC-MS/MS.

Elemental Analysis:

Method development and validation of analytical methods by ICP-MS as per USP<232> and USP <233> for oral solids, Parenteral and Inhalation products.

Quality Policy

We stand committed to good professional practices and compliance by creating a dynamic work culture and ensuring the timely delivery of an industry-leading customer service to all our customers.

We stand committed to work for excellence and ensure providing reliable knowledge of parameters with due compliance to applicable regulations to ensure the quality of operations in its testing, examination, and research services in confirmation to the best of satisfaction of our customers.

We stand committed to work and deliver our services to our customers, in compliance with applicable regulations and agreement by way of orienting and improving our Management System.

We stand committed to ensure that our Quality Management system reaches to the highest level of satisfaction of our customers and regulatory provisions and provides confidence and expertise at all steps of our testing process by continuous monitoring and ensuring continual improvements as would be required under the regulations to head towards an effective Quality Management System that can cater to the needs of all challenges in the working procedure and help developing the strategic indicators for reviewing the system.

We stand committed to continually improve the effectiveness of the management system through the use of quality objectives, audit results, analysis of data , Preventive actions and management review.

We stand committed to work in complete co-operation with our customers with national and international standards of requirements at all the stages of our operation and ensure impartiality, confidentiality and independence in the area of test results evaluation.

We stand committed to evaluate frequently the delivery (customer valued) processes by way of customer-needs mapping and improved with reference to turn around times and “on time in full” service efficiency measurements.

We stand committed to adopt the statistical control techniques to ensure that Quality Improvement Processes are implemented with the help of collection of feedback from customers along with our internal and external audit processes.

Receive News

Subscribe for the Updates!