PCRND delivers end-to-end contract research, API development, and generic drug manufacturing — helping pharmaceutical companies worldwide bring safe, affordable medicines to market faster.
PCRND is a science-led, service-driven pharmaceutical contract research and development organisation with over two decades of expertise across the pharma value chain. Our relentless focus on quality, compliance, and cost-effectiveness makes us the preferred CRO and CMO partner for generic drug developers across India and global regulated markets.
From state-of-the-art API synthesis and formulation development to robust technology transfer and regulatory submission support, our multidisciplinary team delivers results that exceed expectations — and bring better medicines to more patients.
To partner with pharmaceutical innovators and generic drug companies worldwide, delivering scientifically rigorous contract research and development services that accelerate the availability of safe, effective, and affordable medicines for patients in every market.
To be recognised as South Asia's most trusted pharmaceutical contract research and development organisation — a Centre of Excellence that sets the benchmark for quality, innovation, and regulatory compliance in generic drug development by 2028.
Scientific integrity, regulatory excellence, and a patient-first mindset form the foundation of everything we do. Our core values — transparency, quality without compromise, collaborative innovation, and ethical conduct — guide every decision from bench to commercialisation.
From early-stage API research to commercial-scale manufacturing, our comprehensive service portfolio supports every phase of your pharmaceutical product lifecycle.
High-quality pharmaceutical, nutraceutical, and speciality healthcare products for global markets.
Whether you are a multinational pharma company, regional generic drug maker, or biotech startup, PCRND offers flexible engagement models tailored to your goals.
We guide your product from proof-of-concept through pilot-scale feasibility all the way to full commercial manufacturing — managing regulatory milestones, process validation, and supply continuity every step of the way.
Leverage our curated network of GMP-certified contract manufacturing organisations across India and Southeast Asia to find the right CMO partner, negotiate terms, and manage quality oversight on your behalf.
Full-service bioavailability and bioequivalence study management for ANDA and generic drug applications — from protocol design and site selection to data analysis, statistical evaluation, and regulatory submission.
A science-led pharmaceutical contract research and development organisation committed to quality, innovation, and patient-first values across every market we serve.
PCRND (Pharma Contract Research & Development) is a service-based pharmaceutical company with a bold vision for the future of generic medicines. With decades of deep industry experience, our organisation is built on an unwavering commitment to patient health, safety, and access to affordable, high-quality pharmaceutical products.
Our state-of-the-art Research and Development facility, combined with strategic collaborations with GMP-certified manufacturing partners, enables us to deliver Active Pharmaceutical Ingredient (API) development, finished product development, technology transfer, regulatory management, strategic sourcing, and export-ready products to clients across the globe.
We are a multidisciplinary team of scientists, regulatory specialists, manufacturing experts, and business development professionals. Our greatest strength is collaborative teamwork — and our greatest commitment is delivering quality products with an unwavering customer focus.
Partnering with pharmaceutical companies globally to provide world-class contract research and development services — delivering affordable, high-quality medicines that positively impact patient lives and healthcare systems worldwide.
To become the most trusted and preferred pharmaceutical contract research and development service partner in the region by 2028 — recognised for scientific rigour, regulatory excellence, and the quality of every product that leaves our facility.
We trust in the principle: when your values are clear, decision-making becomes straightforward. Our values are classified into two core categories — Core Values that define who we are, and Business Values that define how we operate and serve our partners and patients.
Our management is anchored on three core values that motivate our teams to grow effectively, maintain the highest standards, and deliver meaningful outcomes for our partners and the patients they serve.
We uphold the highest ethical standards in all operations. Protecting and advancing the regulatory requirements and quality procedures essential to producing safe, effective drug products is non-negotiable at every level of our organisation.
Our diverse team of subject-matter experts in R&D, manufacturing, regulatory affairs, and business development works as one cohesive unit. We believe that collaborative teamwork is the engine behind every successful project and partnership.
We actively seek and welcome feedback from customers, partners, and stakeholders. Every complaint, every suggestion, and every data point is an opportunity to improve our processes, products, and services — accelerating our journey towards excellence.
Every PCRND team member is bound to practise these business values to deliver the best possible service to our pharmaceutical partners and end-users.
We are committed to the delivery of quality healthcare products worldwide. Our robust processes, validated methods, and GMP-compliant systems consistently exceed the expectations of our partners and end-users.
We are dedicated to serving human life. Our work is guided by a deep respect for patients, partners, and communities — giving back to society through medicines that make a real difference to those who need it most.
We are deeply committed to understanding and exceeding our business partners' expectations. Customer satisfaction drives every decision — we deliver what we promise, on time, and to the quality specification agreed.
We build trust-based relationships with our partners that transcend transactional interactions. Strong collaboration is how we achieve mutual business success and advance our shared mission of improving global patient health.
Comprehensive pharmaceutical contract research and development services — from small molecule API synthesis to commercial manufacturing — tailored to accelerate your product pipeline.
At PCRND, we specialise in solving your API development challenges to accelerate your molecule through early-phase trials and achieve industry-leading performance. Partner with us for quality and excellence in small molecule development — whether you need milligram quantities for initial feasibility work or multi-kilogram batches for a late-phase clinical trial.
PCRND provides comprehensive formulation development services for generic drug products destined for regulated and semi-regulated markets. Our experienced scientists tackle the most complex bioavailability, stability, and solubility challenges to develop robust, commercially viable dosage forms.
PCRND provides deep expertise and operational agility for technology transfer throughout the drug product lifecycle. Our trusted approach ensures a quicker, simpler, and seamless transfer process with full documentation support at every stage. Our experienced team enables efficient, successful transfers while maintaining regulatory continuity and production quality.
PCRND offers a one-stop solution for conducting Bioequivalence Studies and Clinical Trials in India. Indian CROs are globally recognised for their regulatory-compliant systems, competitive study costs, and timely completion. PCRND helps you select experienced, accredited CROs to maximise your cost-effective study outcomes.
PCRND provides clinical trial material and commercial supply manufacturing services to pharmaceutical organisations of all sizes. Our range of specialist capabilities and strategic CMO collaborations cover regulatory and semi-regulatory categories including prescription, OTC, nutraceuticals, and cosmetic products.
PCRND sources high-quality, cost-effective active pharmaceutical ingredients and excipients to meet each client's specific needs. Our global sourcing strategy is built around your business requirements. We manage a worldwide network of audited manufacturers, ensuring compliance status and uninterrupted supply — reducing your product development lifecycle by 20–30%.
Our sourcing portfolio covers: API · Excipients · Packaging Material · Ready-to-Compress Granules · Ready-to-Fill Pellets
PCRND uses advanced Patent Databases and Analytics Tools for customised Business Research projects — including Competitive Landscapes, Technology Research (state-of-the-art and White Space Analysis), and Legal Research (Patentability, Evidence of Use, Validity/Invalidity, FTO and Third-Party Patent Clearance).
PCRND operates a state-of-the-art small molecule finished-product development and technology transfer facility — available for own projects and client manufacturing sites. Our GMP-approved Centre of Excellence is fully equipped for development of generic products, reformulation, and life cycle extension. We deploy Process Analytical Technologies (PAT) and Quality-by-Design (QbD) tools to deliver superior pharmaceutical products efficiently.
| Dosage Form | Category | Target Market | Development Status |
|---|---|---|---|
| Immediate Release Tablets | Solid Oral | USA, EU, ANZ | Active |
| Modified/Extended Release Tablets | Solid Oral | USA, EU | Active |
| Hard Gelatin Capsules | Solid Oral | USA, EU, ANZ | Active |
| Oral Liquid Suspensions | Liquid | EU, Emerging Markets | Active |
| Topical Creams & Ointments | Semi-solid | Global | Active |
| Transdermal Patches | Specialty | USA, EU | In Development |
| Nutraceutical Softgels | Specialty | Global | Active |
| Ophthalmic Drops | Sterile | EU, ANZ | In Development |
Compliant with World Health Organization Good Manufacturing Practice standards
Chilean Ministry of Health approved facility for pharmaceutical exports
Department of Drugs and Food (DDF) Cambodia approved
National Agency for Food and Drug Administration and Control approved
PCRND is committed to providing world-class quality medicines at affordable prices. We have established a culture of manufacturing excellence from day one and sustain it through continuous investment, skill development, and agile operations.
Manufacturing excellence is embedded in our DNA — not merely a compliance checkbox. Every batch, every record, every decision reflects our commitment to producing medicines that patients and healthcare providers can trust.
Our manufacturing environments are designed to global GMP standards with state-of-the-art equipment, robust environmental monitoring, and validated cleaning processes that ensure product quality and patient safety.
We apply Lean, Six Sigma, and CAPA-driven approaches to continuously enhance process efficiency, reduce deviations, and improve overall equipment effectiveness across all manufacturing operations.
Our people are our greatest asset. Structured training programmes, competency assessments, and ongoing professional development ensure our team operates at the cutting edge of pharmaceutical manufacturing science.
Rigorous quality management systems, in-process controls, and comprehensive release testing guarantee every product meets the specification defined in the registered dossier — every time, without exception.
Flexible manufacturing protocols allow us to respond rapidly to client needs, market changes, and supply chain demands — reducing lead times and ensuring uninterrupted commercial supply for our global customers.
Discover our growing portfolio of high-quality pharmaceutical, nutraceutical, herbal, cosmetic, and over-the-counter products developed for domestic and global regulated markets.



















Showing all 19 products from our current catalogue. Contact us to inquire about pipeline products, custom development, and bulk supply.
Our clients and their pharmaceutical projects benefit from PCRND's deep industry resources and scientific expertise. We commit to partnerships that make a significant, lasting impact on patient health worldwide.
Our ideal partner shares our commitment to breakthrough pharmaceutical science and a vision to make a lasting contribution to people's health. Whether you are seeking a contract research organisation, a manufacturing connection, or clinical study management, PCRND offers structured, transparent engagement models that deliver results.
We operate across three primary partnership types, each with a clearly defined process, mutual obligations, and shared milestones — so you always know where your project stands.
We take your molecule from initial proof-of-concept through every development milestone to full commercial manufacturing supply. This partnership model is ideal for companies seeking a single, accountable partner for the full development journey.
Leverage PCRND's extensive network of audited, GMP-certified contract manufacturing organisations. We act as your qualified representative in India — finding the right CMO partner, negotiating on your behalf, and ensuring quality product supply throughout the relationship.
PCRND manages your complete bioavailability and bioequivalence study journey — from identifying the right accredited CRO to managing the study and delivering the final report for your regulatory submission. India offers globally competitive BA/BE study costs with rigorous GCP compliance.
People are our greatest asset. We invest in talent, foster a culture of growth, and offer a stimulating environment where science, innovation, and patient health intersect every day.
At PCRND, we are always open to attracting exceptional talent who want to be part of an exciting pharmaceutical success story. If you have the skills, drive, and passion to achieve the very best — we will provide the platform, mentorship, and opportunity to grow.
We offer a dynamic, vibrant work culture where collaboration, continuous learning, and scientific curiosity are celebrated. From fresh graduates to seasoned pharma professionals, PCRND is the place where careers flourish and contributions matter.
Access to cutting-edge R&D projects, continuous learning programmes, and mentorship from industry-leading scientists and regulatory experts.
An inclusive, collaborative work environment that values every team member's contribution and celebrates scientific curiosity and innovation.
Structured career pathways, performance-linked growth, and opportunities to lead high-impact pharmaceutical projects from day one.
Market-competitive compensation, health benefits, flexible policies, and recognition programmes that reward excellence and dedication.
Work on projects for regulated markets including the USA, EU, and Australia — gaining valuable international pharmaceutical development experience.
Every project ultimately contributes to making safer, more affordable medicines accessible to patients worldwide — work that truly matters.
We are always looking for exceptional talent across Research & Development, Regulatory Affairs, Manufacturing, Quality Assurance, Business Development, and more. Send us your details and we will be in touch when an opportunity matching your profile arises.
Current focus areas: API Scientists, Formulation Scientists, Regulatory Affairs Specialists, QA/QC Analysts, Business Development Managers.
📧 Direct Applications
You may also send your CV directly to pcrndin@gmail.com
Whether you have a partnership enquiry, a product question, or simply want to learn more about PCRND's capabilities — our team is ready to assist.
We welcome enquiries from pharmaceutical companies, biotech organisations, academic researchers, and healthcare professionals worldwide.
Tirunelveli Junction,
Tirunelveli – 627 006,
Tamilnadu, India
Palayamkottai,
SIPCOT,
Palayamkottai, Tirunelveli – 627002, Tamilnadu, India