Our Services

GenesisCrest is a leading service provider of custom research solutions, providing expert R&D, clinical, regulatory and market research services to medical device, pharma and healthcare product manufacturers.

We provide scientific intelligence, and strategic support during every stage of the product development process to get medical products commercialized early in the major markets across globe.

Efficient, customized scientific services across full spectrum of product design and development

At GenesisCrest, we provide customized scientific services incl. regulatory and reimbursement expertise in global markets that bring clarity and direction to your process thus help you gain confidence in your projects and get edge over the competition.

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We strive to become a trusted partner, and ensure this by providing uncompromized quality deliveries on time with the help of right mix of talent and skill.

Our sole focus on Life sciences and MedTech enables us to provide informed, customized, actionable strategic insights that draw on our robust problem solving methodologies.

Our unique approach of defining customer requirements, market analysis and competitive assessment can help you move quickly from concept to launch.

Delivering a medical product to market can be a long and complicated process, even when you’re familiar with the regulatory requirements and market dynamics. Our proven and results-oriented approach can help you achieve multiple efficiencies throughout the development, market approval, market access phase across the globe.

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Our vision is to offer a wide range of customized research services necessary to take a medical product from concept through post regulatory approval.

Our team have unique ability to analyze complex medical information and data to prepare complex documents and publications in accordance with relevant guidelines. We can help you prepare clear, concise, and high quality reports and documents for regulatory submissions, and effective marketing communications.

Our medical writers organize, interpret and present data in an accurate, professional and trusted manner that is well recognized and trusted by global regulatory entities.

We integrate these services in unique ways that could truly save time and cost to client by complementing client teams with additional skill set and helping them focus on main development/market priorities. Our broad expertise spans key product development disciplines and expanded global reach enables up delivering value to our clients.

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We provide specialized report writing, and evidence communication services to support clinical and regulatory objectives.

What We Do

Founded by professionals from the pharmaceutical and medical device sector, GenesisCrest provide unique blend of business, domain, technology, and product (drug/device) development expertise.

Our techno-commercial experience, both in-house and through our network of associates, cover all forms of drug/device development research – qualitative and quantitative. We specialize in providing services related to R&D due-diligence, competitive assessment and market intelligence for healthcare organizations (medical device, pharmaceutical, biotech and specialty life sciences).

For further information, please visit About Us page.

What-we-do

Industries We Serve

Medical Devices

Device classification, Regulatory submissions (510K, CE), CER report writing. Learn more

Diagnostics

Biomarkers identification and validation, Technology evaluation, Market assessment. Learn more

Pharmaceuticals

Drug target identification and validation, literature reviews, pipeline assessment, clinical trial analytics. Learn more

Life Sciences

Research protocols, Grant proposals, CER report writing, Business plans, Technical report writing. Learn more

Reasons to Work Together

Have questions on what GenesisCrest can do for you?
We welcome the opportunity to continue the discussion.