Product Development Focus

We offer end-to-end support for In-Vitro Diagnostic (IVD) kit development, covering assay design, reagent optimization, prototype creation, analytical validation, and regulatory documentation to ensure high accuracy, reliability, and global compliance. Our scientific expertise and quality-focused approach help transform diagnostic concepts into robust, scalable, and market-ready kits with streamlined workflows and dependable performance.

 

In-vitro diagnostic kit development

Medical device manufacture

We provide comprehensive support for the manufacturing of medical devices, ensuring each product meets stringent quality, safety, and regulatory standards. Our capabilities span process design, material selection, prototyping, validation, and scalable production, supported by robust quality management systems. With a focus on precision, compliance, and efficiency, we help bring reliable, high-performance medical devices to market with confidence.
 

 

Botulinum toxin a based cosmetics development and manufacture

We offer specialized expertise in the development and manufacture of Botulinum Toxin A–based cosmetic products, ensuring scientifically robust formulations, controlled potency, and strict compliance with global regulatory standards. Our capabilities include strain selection, fermentation, purification, formulation optimization, aseptic fill-finish, and stability evaluation, all supported by validated processes and high-level quality systems. With a focus on safety, precision, and performance, we help deliver high-quality Botulinum Toxin A cosmetic products that meet market expectations for efficacy and reliability.

 

Key Capabilities

We have a strong foundation and technical expertise which includes product development, scale-up, process optimization for bio-pharmaceuticals, vaccines and medical devices

A deep understanding of regulatory frameworks and compliance requirements for navigating the complex regulatory landscape in the biotech industry with domain expertise in EU/ FDA regulations, Good Manufacturing Practices (GMP), and clinical development.

We have the ability to conduct comprehensive market research and analysis for assessing market trends, competition, and potential opportunities for clients. This involves gathering and interpreting data, conducting market assessments, and providing strategic recommendations.

We possess strong business acumen and strategic thinking for assisting clients with business planning, market entry strategies, commercialization plans, and financial analysis.

Expertise in intellectual property rights, patent analysis, and technology transfer to help protect inventions, assess patent landscapes, and develop IP strategies.

We assist clients with due diligence and valuation processes for mergers, acquisitions, licensing agreements, and investments.

Project management skills for successfully executing biotech projects. This involves managing timelines, resources, budgets, and cross-functional teams to ensure the successful completion of client projects.

Effective communication and presentation skills to convey complex scientific and technical information in a clear and concise manner. This includes preparing reports, delivering presentations, and engaging with clients and stakeholders.

Building collaborative relationships and networks within the biotech industry which allows for partnerships, knowledge sharing, and access to key stakeholders and experts.

Services based on 6P Principle

POTENTIAL

Assessment of market potential
detailed project feasibility studies

PRODUCT

Identify right products for apt portfolio

PLANT

Turnkey project construction through strategic partners

PARTNERSHIP

Enable best fit partnerships to source technology and finished products

PEOPLE

Enable recruitment of best talent to manage plant and product portfolio

PROFITS

Ensure consistent profits with constant support to address the first five P’s

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