Product Development
Advance concepts into commercial-ready generic and hybrid products with formulation optimization, analytical method development, scalable batch manufacturing, technology transfer, and eCTD dossier preparation.
DRK Research Solutions delivers integrated CDMO support that moves generic and hybrid pharmaceutical products from formulation strategy to commercial-ready supply. Our scientific, regulatory, and manufacturing expertise helps pharmaceutical and biopharmaceutical organizations coordinate critical development activities, reduce handoffs, and prepare for regulated-market submissions. Partner with a globally connected team focused on quality, speed, and expanded patient access to modern therapies.

Integrated development, manufacturing, regulatory, and compliance support for pharmaceutical products progressing toward regulated global markets.
Advance concepts into commercial-ready generic and hybrid products with formulation optimization, analytical method development, scalable batch manufacturing, technology transfer, and eCTD dossier preparation.
Build robust lab-scale formulation strategies grounded in scientific precision, product performance goals, manufacturability, and regulatory foresight for development programs.
Develop and validate analytical methods that support product quality, safety, consistency, and the documentation expectations of regulated-market submissions.
Coordinate the transfer of product knowledge, processes, and technical requirements to manufacturing facilities or CMOs while protecting consistency and scalability.
Support exhibit and commercial batch manufacturing aligned with global regulatory standards, helping programs move from development through market-ready supply.
Prepare compliant dossiers, support eCTD submissions, and provide in-licensing or out-licensing documentation for regional and international market opportunities.
A successful product program requires more than isolated development tasks. DRK Research Solutions connects formulation, analytical development, technology transfer, manufacturing, regulatory documentation, and compliance planning in one strategic CDMO pathway. Our team supports generic and hybrid products for regulated markets while maintaining a clear focus on product quality, scalable execution, and timely progress. This coordinated approach helps sponsors make informed decisions from early development through commercial supply readiness.

We align scientific rigor, global reach, and patient-centered priorities across every development milestone.
Connect development, manufacturing, regulatory, and clinical capabilities through one coordinated strategic partner.
Access worldwide operational networks with localized proficiency across Europe, Asia, Africa, the Middle East, and Americas.
Focused project coordination and rapid execution help maintain momentum across critical product development activities.
Advance therapies with a mission centered on expanding access for underserved populations worldwide.
Scientific, medical, and strategic leaders supporting every development stage.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
End-to-end CDMO services combine the key activities needed to move a pharmaceutical product toward market readiness. At DRK Research Solutions, support can include formulation development, analytical method development, technology transfer, exhibit and commercial batch manufacturing, eCTD dossier preparation, and regulatory support. Integrating these functions helps sponsors coordinate decisions, documentation, timelines, and quality expectations across the product lifecycle.
Speak with our team about your product development priorities.
Quality-focused support for regulated pharmaceutical development programs.
Worldwide reach with localized operational proficiency.
Focused on broader access to modern therapies.
Share your program goals and current development stage. Our team will help identify the CDMO support best suited to your regulatory and commercialization objectives.
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.
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.