mPEG Development and CDMO Services for Drug Manufacturing

DRK Research Solutions delivers integrated mPEG development and CDMO services that move generic and hybrid drug products from formulation strategy to commercial-ready supply. Our multidisciplinary team combines scientific rigor, analytical development, technology transfer, and regulatory-ready documentation to help pharmaceutical and biopharmaceutical organizations shorten development timelines while maintaining quality, consistency, and market-readiness across regulated markets worldwide.

Scientists reviewing pharmaceutical formulation samples

Our mPEG Development and CDMO Services

Integrated development, manufacturing, and regulatory support for market-ready generic and hybrid pharmaceutical products.

CDMO Services

End-to-end contract development and manufacturing support for pharmaceutical companies and marketing organizations developing high-quality generic and hybrid products for regulated markets.

Product Development

Lab-scale formulation development, optimization, analytical method development, technology transfer, and exhibit or commercial batch manufacturing designed for scalable, compliant product progression.

Regulatory Support

Product dossier out-licensing, in-licensing support, eCTD submissions, and regulatory documentation that help prepare products for efficient review across regional and international markets.

End-to-End Development

Advance Drug Products With Greater Confidence

From early formulation design through commercial-ready manufacturing support, DRK Research Solutions helps sponsors create a practical path to regulated markets. Our mPEG development and CDMO services connect formulation optimization, validated analytical methods, technology transfer, batch manufacturing, and eCTD dossier preparation. This coordinated model reduces handoffs, supports consistent scale-up, and gives generic and hybrid product teams focused scientific and regulatory support at every critical stage.

Pharmaceutical team evaluating drug development data
The DRK Difference

Why Choose DRK Research Solutions?

A connected global partner for scientifically rigorous, patient-focused pharmaceutical development.

Integrated Expertise

Connect development, manufacturing, clinical, and regulatory capabilities through one coordinated global partner.

Regulated Market Focus

Support generics and hybrid products with regulatory-aware development built for demanding market requirements.

Global Local Reach

Worldwide networks and localized proficiency help sponsors navigate diverse regional needs and partnerships.

Timely Delivery

Focused project coordination helps shorten development timelines without losing sight of quality.

Meet the DRK Leadership

Experienced leaders guiding global pharmaceutical development and access.

Portrait of Dr. Shahab Q. Khokhar, Executive Director at DRK Research Solutions

Dr. Shahab Q. Khokhar

Executive Director

Dr. Shahab Q. Khokhar serves as Executive Director at DRK Research Solutions SA, bringing strategic leadership and deep pharmaceutical expertise to the organization's global operations. With a career rooted in clinical research and pharmaceutical development, Dr. Khokhar has been instrumental in shaping DRK's growth from a Patient Advocacy Organization into a full-service CRO and CDMO. He provides executive oversight across multi-regional clinical trials, regulatory compliance, and business strategy, ensuring the company upholds the highest GxP and ethical standards. His vision drives DRK's commitment to expanding access to innovative therapies, particularly for underserved populations across LMICs in Europe, the Middle East, Asia, Africa, and the Americas.

Portrait of Azka Wase, Head of Business Development at DRK Research Solutions

Azka Wase

Head Of Business Development

Azka Wase is the Head of Business Development at DRK Research Solutions SA, responsible for driving strategic partnerships and expanding the company's global client base across the pharmaceutical and biopharmaceutical sectors. With a strong foundation in life sciences and commercial strategy, Azka leads efforts to connect sponsors, research institutions, and healthcare partners with DRK's end-to-end CRO and CDMO capabilities. Her work spans DRK's operational regions, including Europe, the Middle East, Asia, Africa, and the Americas. Azka is committed to building meaningful, long-term collaborations that accelerate drug development timelines and ultimately improve patient access to innovative treatments worldwide.

Portrait of Vipan Dhall, Ph.D., Chief Scientific Officer at DRK Research Solutions

Vipan Dhall, Ph.D.

Chief Scientific Officer

Vipan Dhall, Ph.D., serves as Chief Scientific Officer at DRK Research Solutions SA, leading the company's scientific strategy and innovation agenda. With advanced expertise in pharmaceutical sciences, Dr. Dhall oversees the scientific direction of clinical development programs and CDMO services, including generics and hybrid product development for regulated markets. He plays a central role in ensuring that DRK's research methodologies meet the highest standards of scientific rigor and regulatory compliance. Dr. Dhall is passionate about leveraging cutting-edge science and technology to bring therapies to patients faster, consistent with DRK's core value of innovation with purpose and its mission to enhance global healthcare access.

Portrait of Dr. Isabel Potani, PhD, Clinical Trials Implementation Specialist at DRK Research Solutions

Dr. Isabel Potani, PhD

Clinical Trials Implementation Specialist

Dr. Isabel Potani, PhD, is a Clinical Trials Implementation Specialist at DRK Research Solutions SA, bringing specialized expertise in the design, coordination, and execution of clinical trials across diverse international settings. With a particular focus on multi-regional clinical trials, Dr. Potani ensures rigorous implementation standards are maintained from site initiation through study completion. Her background and dedication to patient-centric research make her especially effective in trials targeting underserved and LMIC populations. Dr. Potani collaborates closely with global sponsors, site investigators, and regulatory bodies to deliver high-quality clinical data while prioritizing participant safety and study integrity throughout every phase of the trial process.

Portrait of Dr. Zenaida Reynoso-Mojares, Chief Medical Officer at DRK Research Solutions

Dr. Zenaida Reynoso-Mojares

Chief Medical Officer

Dr. Zenaida Reynoso-Mojares serves as Chief Medical Officer at DRK Research Solutions SA, providing senior medical leadership across the company's clinical development portfolio. With extensive experience in clinical medicine and pharmaceutical research, she oversees medical strategy, patient safety, and the medical integrity of DRK's clinical trial programs from Phase II through Phase IV. Dr. Reynoso-Mojares ensures that all clinical activities adhere to the highest GxP, ethical, and regulatory standards across DRK's global operational regions, including Europe, the Middle East, Asia, Africa, and the Americas. Her patient-centric philosophy aligns with DRK's core mission of improving healthcare access for underserved populations worldwide.

Portrait of Dr. Onesmo Mpanju, Regional Head USA & Africa at DRK Research Solutions

Dr. Onesmo Mpanju

Regional Head – USA & Africa

Dr. Onesmo Mpanju is the Regional Head for USA & Africa at DRK Research Solutions SA, leading the company's strategic operations and business development activities across two of its most impactful regions. With a strong background in pharmaceutical research and regional healthcare systems, Dr. Mpanju manages DRK's presence at its Aldie, Virginia office while fostering key relationships with sponsors, research institutions, and healthcare partners across the African continent. His expertise in navigating diverse regulatory environments and his dedication to expanding clinical research capabilities in underserved African markets directly support DRK's mission to enhance global healthcare access, particularly for low- and middle-income country populations.

Portrait of Dr. Zafar Mirza, Senior Strategic Advisor at DRK Research Solutions

Dr. Zafar Mirza

Senior Strategic Advisor

Dr. Zafar Mirza brings distinguished expertise to DRK Research Solutions SA as Senior Strategic Advisor, providing high-level guidance on global health policy, regulatory strategy, and pharmaceutical development. With a career spanning international health organizations and pharmaceutical research, Dr. Mirza offers invaluable insight that helps shape DRK's long-term strategic direction. His advisory role supports the company's mission to bridge global healthcare gaps and improve access to modern treatments, particularly in underserved regions. Dr. Mirza's deep knowledge of global regulatory landscapes and his commitment to equitable healthcare access make him a cornerstone of DRK's leadership team and an essential voice in the company's patient-centric philosophy.

Portrait of Dr. Nigel Whittle, Country Head UK at DRK Research Solutions

Dr. Nigel Whittle

Country Head UK

Dr. Nigel Whittle serves as Country Head UK for DRK Research Solutions SA, overseeing all operations and business activities from the company's Cambridge, United Kingdom office. With extensive experience in the UK pharmaceutical and clinical research landscape, Dr. Whittle manages local stakeholder relationships, regulatory engagements, and business development across the United Kingdom and broader European markets. He ensures that DRK's UK operations maintain the highest standards of compliance and service delivery consistent with the company's global reputation. Dr. Whittle's localized expertise combined with DRK's worldwide capabilities enables seamless delivery of CRO and CDMO services to pharmaceutical and biopharmaceutical clients across Europe.

Portrait of Muhammad Mazree, Regional Head Southeast Asia at DRK Research Solutions

Muhammad Mazree

Regional Head - Southeast Asia

Muhammad Mazree is the Regional Head for Southeast Asia at DRK Research Solutions SA, directing the company's operations and growth strategy from its Shah Alam, Selangor, Malaysia office. With deep knowledge of the Southeast Asian pharmaceutical market, regulatory environment, and clinical research ecosystem, Muhammad manages key regional partnerships and oversees business development activities across this dynamic and rapidly growing market. He ensures that DRK's global CRO and CDMO capabilities are effectively delivered to local pharmaceutical and biopharmaceutical clients while maintaining the company's exacting standards of quality and compliance. His regional leadership is critical to DRK's mission of expanding healthcare access across Asia.

Portrait of Krishnaveni Thanappan, Clinical Data Manager at DRK Research Solutions

Krishnaveni Thanappan

Clinical Data Manager

Krishnaveni Thanappan is a Clinical Data Manager at DRK Research Solutions SA, specializing in the collection, management, and quality assurance of clinical trial data across DRK's global studies. With expertise in data management systems and regulatory-compliant processes, Krishnaveni ensures the integrity, accuracy, and completeness of clinical data from trial initiation through database lock. Her meticulous approach supports DRK's commitment to delivering high-quality evidence that meets the rigorous standards of global regulatory agencies. Krishnaveni works collaboratively with clinical operations, biostatistics, and sponsor teams to maintain seamless data flows, contributing directly to the success of multi-regional clinical trials and the advancement of innovative pharmaceutical therapies.

Portrait of Maha Fareed, Lead PMD & OD at DRK Research Solutions

Maha Fareed

Lead PMD & OD

Maha Fareed serves as Lead Project Management & Organizational Development (PMD & OD) at DRK Research Solutions SA, driving the effective planning, execution, and delivery of the company's complex pharmaceutical and clinical research projects. With a strong background in project management and organizational development, Maha ensures that DRK's cross-functional teams operate with efficiency, cohesion, and strategic alignment across its global offices. She plays a vital role in building internal capabilities and streamlining processes that support timely project delivery—one of DRK's key competitive advantages. Maha's commitment to fostering a diverse, inclusive, and high-performing workplace reflects DRK's core values and its vision for sustainable organizational growth.

Frequently Asked Questions

What does CDMO services mean?

CDMO services are provided by a Contract Development and Manufacturing Organization. A CDMO supports pharmaceutical companies with activities such as formulation development, analytical method development, technology transfer, manufacturing scale-up, batch production, and regulatory documentation. Instead of building every capability internally, a sponsor can work with a CDMO to access specialized expertise and coordinated support from product concept through commercial supply preparation.

What is the difference between a CMO and a CDMO?

What is the difference between a CRO and a CDMO?

What types of products can CDMO services support?

When should a sponsor engage a CDMO?

How does technology transfer support drug manufacturing?

What regulatory support is available for product development?

How can CDMO services help reduce development timelines?

Have Questions About Your Program?

Speak with our team about your drug development priorities.

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GxP Compliance Support

Regulatory-focused quality and compliance guidance

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Global Network

Worldwide reach with localized proficiency

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Over a Decade

Pharmaceutical expertise since 2012

Build Your Path to Market Readiness

Share your product goals and development requirements. Our team will help identify the right CDMO support pathway for your program.

Contact Us Today

For immediate assistance, feel free to give us a direct call at +41 76 797 25 67. You can also send us a quick email at info@drkresearch.com.