Chromex | HPLC, GC Training, Student Project Work | HPLC, GC Training, Student Project Work

Chromex Research Laboratories, is committed to —

We, at Chromex Research Laboratories, are committed to provide prompt and efficient analytical services, meeting the legitimate requirements of our customer as well as the regulatory authorities. We will maintain high quality standards by continuous improvement in all operations through appropriate training, constant reviews, and participation of all the employees and by the way of technological advancement. All the personnel concerned with testing shall be trained for the quality documentation and implementing the policies and procedures in their work. We will strive to improve customer confidence in us, by way of constant interaction and feedback.
To providing the highest quality analytical data that meets the needs of our clients and is defendable, ethical, accurate and independent. Our commitment is supported by effective quality systems, current technology, technical expertise and efficient customer service.

“CUSTOMER SATISFACTION IS OUR MOTTO.”

Analytical tests are developed to support the entire drug development process, and tests are required for all phases of the drug development process: lead candidate selection, manufacturing of a new drug, quality control, quality assurance and more.
These all-important tests must be qualified and then verified and be validated for testing; they must be in accordance with international standards for conducting tests for medical products. All tests need to be cost-effective to optimize the development of your new drug or API. The best way to achieve this is to outsource to a reliable cGMP laboratory.
Take advantage of the right methods for your product at each stage of the development cycle to develop a safe, reliable and efficient pharmaceutical product.

Gain an experienced partner with a good working knowledge of method validation requirements suitable for different phases of development. Chromex Analytical respects the highest standards of the pharmaceutical industry by following relevant ICH guidelines such as ICH Q2 (R1) or Pharmacopoeial methods/compendia guidance in combination with client-specific protocols.

A forced degradation study investigates the stability of a chemical or pharmaceutical product under stressful conditions (forced degradation research is also known as stress testing). “Stress” in this case means any physical or environmental conditions that a product will encounter that could cause a chemical change.

The understanding and the supportive nature will help you to improve of your knowledge and interest. I like the way of teaching.

Hemrajsinh RathodFreshers

Excellent experience regarding Analytical Method development and Validation services in stipulated time.

Sachin PatelQA Head - Apex healthcare

Very good on site support with excellent technical skills.

You will be much free to discuss and to raise your voice.

Vijay YadavQA Head - Amsal Chem

Excellent knowledge for Analytical Method development and Validation.

Umesh PatelQC Head

We are happy to assist you if you have any queries regarding any of our Services or Courses.