Chorus Life Sciences LTD.

Regulatory Affairs

Overview

Regulatory Affairs

Chorus Life Sciences Ltd is not just a team of specialists for formulating pharmaceuticals and nutraceuticals. We aim to develop a platform where healthcare experts and pharmaceutical researchers can strengthen their knowledge. So, we have created this page to keep you up-to-date about the latest happenings in the pharmaceutical industry. You will have a detailed insight into the medical world. Visit this page every day and find the regular news from the single platform.

Our Events

Chorus Life Sciences Ltd has established connections with different regulatory bodies.

ACTD (ASEAN Common Technical Dossier)-

As we run our business in Asian countries, we register our products in the ASEAN member states. Our team goes through various steps to get the healthcare products approved.

CTD (Common Technical Document)

CTD is the standard format for our pharmaceutical company’s regulatory submission. It allows us to release our medical products in the EU and US markets. We submit every detail about our quality and safety maintenance initiatives. Our industry specialists and pharmacists efficiently present the products in a compliant way to pass the regulatory evaluation process.

eCTD (Electronic Common Technical Document)

By leveraging the eCTD format, we accelerate the regulatory submission process. The electronic procedure ensures a quicker review and instant approval. So, it helps us market our pharmaceutical and nutraceutical products shortly.

Our regulatory affairs enable us to dominate the local markets in various countries. With our expertise, we manage a smooth product lifecycle. Our strong knowledge lets us deal with industry-related complexities. You can rely on our compliant products to operate your business in the healthcare world.

Why Choose

Chorus Life Sciences for Global Partnerships?

Excellence and Value converge for superior quality medications at Chorus Life Sciences Ltd.