Amber Lifesciences Iceland

Amber LifeSciences operates in Iceland, partnering with the Icelandic Medicines Agency under the Ministry of Health. We offer CMO, CDMO, and CRO services, focusing on Oral, Liquid, Injectable, and Biological formulations for the pharmaceutical market.

Iceland

In collaboration with WHO-cGMP, USFDA, and EUGMP-accredited organizations, Amber LifeSciences ensures regulatory compliance and a reliable pharmaceutical supply in Iceland. We specialize in providing competitive pricing and expertise in Oral, Liquid, Injectable, and Biological formulations to meet Iceland’s healthcare needs.

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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