Amber Lifesciences Kazakhstan

Amber LifeSciences is dedicated to enhancing healthcare in Kazakhstan, collaborating with the Ministry of Health and the Committee for Control of Medical and Pharmaceutical Activities for pharmaceutical quality assurance. We specialize in CMO, CDMO, and CRO services, focusing on Oral, Liquid, Injectable, and Biological formulations.

Kazakhstan

Amber LifeSciences aims to improve healthcare access in Kazakhstan through partnerships with the Ministry of Health and the Committee for Control of Medical and Pharmaceutical Activities. We collaborate with WHO-cGMP, USFDA, and EUGMP-accredited partners to ensure reliable supply, competitive pricing, and regulatory expertise. Our comprehensive offerings include CMO, CDMO, and CRO services, ensuring compliance while delivering high-quality products tailored to the healthcare needs of the Kazakh population.

25+ Product Range with Regulatory Support

Amber LifeSciences Offers an Extensive Portfolio of over 25 Product Types & Formulations, backed by comprehensive Regulatory support to ensure a seamless approval process for your healthcare products.

Tablets

Capsules

Lotion

Injection

Eye Drops

Inhaler

Human Albumin

Ointments

Syrup

Nasal Sprays

Infusion

Biological

Expert Regulatory Guidance for Registration

Our dedicated Drug Regulatory Affairs team works closely with you, providing all the necessary documentation and guidance for product registration. With Amber LifeSciences, you can count on expert support and a hassle-free path to regulatory clearance.

50+ Exporting

Countries

7000+ Product

Lines

500+ Clients

Globally

500+ Ready

Dossiers

Why Choose Amber LifeSciences?

Amber LifeSciences provides expert regulatory services, ensuring pharmaceutical products meet global standards with ease. Our dedicated team offers end-to-end support, emphasizing quality, efficiency, and international compliance.

CTD and ACTD Dossiers

Complete documentation for global regulatory submissions.

Essential Certifications

Free Sale Certificate (FSC) and Certificate of Pharmaceutical Product (COPP) for global distribution and approval.

Bioequivalence (BE) Studies

Supporting product approval with essential data and reports.

Product Samples & Analysis

Providing samples, Certificate of Analysis (COA), and product verification for registration.

Post-Approval Support

Ensuring continued regulatory adherence with ongoing support.

Regulatory & Consultation

Expert guidance and tailored documentation for country-specific requirements.

“We Listen, We Care, We Deliver.”

Got Questions? Drop us a Message!

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+91 91370 77377

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