Our core services
Project Management and support to the generic and non-generic pharmaceutical industry.
Why Choose us?
Proven track record in providing innovative and cost effective support.
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Interested in challenging regulatory projects working for major pharmaceutical companies?
JSK RegLink provides dependable global regulatory affairs proficiency and services whereby submissions are managed scrupulously whilst maintaining an efficient approval rate.
With the constant amendments to Regulations, JSK RegLink’s versatility allows all types of submissions to be handled internationally, with the re-assurance that a group of well-trained, experienced and qualified scientific specialists will be there every step of the way.
Stakeholders interests and registration strategies are assessed while local legal regulations and quality are considered throughout the product development process.