Our solutions
Assistance with your product’s Chemistry, Manufacturing, and Controls (CMC) documentation.
LINK Medical handles early clinical studies, including First in Man studies.
Local or international, methodology is our expertise.
Support with all kinds of late phase studies.
Both Prior and post marketing.
Services to ensure the sustained market presence of your product.
In addition to Medical Device Regulations (MDR).
This is here to stay and we have the experience.
Centralizing all safety data in a single system.
A team of senior experts all with different expertise to support you with vital strategic planning.
CTIS application and support during the start-up phase.
Efficient solution for the best use of resources, regardless of the scope.
LINK Medical Solutions
LINK Medical CRO has cutting edge expertise in methodology for all clinical trial phases regardless of the indication or complexity. Our regulatory section is strong both in pre and post marketing services, including CMC and compliance review.
Integrity
A strong Nordic culture underpins our high-quality service based on respect, work integrity and focus on solutions.
Agility & Flexibility
We have the flexibility to deliver the support you need, no matter how big or small your project.
Expertise
Our leading experts and technologies ensure we always follow industry advances and current regulations.
Comprehensive
We offer wide ranging services to pharma and medical device industries for your entire product development journey.
590 +
clinical trials
150 +
employees
20 +
therapeutic areas
6
countries