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Dosage Life Sciences (P) Limited (DLS) is a trusted consultancy and manufacturing partner specializing in the pharmaceuticals, nutraceuticals, and cosmeceuticals sectors.
We offer end-to-end solutions across Greenfield/Brownfield project execution, formulation development, regulatory compliance, and contract manufacturing, empowering clients to achieve excellence in both regulated and emerging markets.
Led by industry veteran Dr. Rajesh K. Singh, who brings over 30 years of leadership experience from top pharmaceutical companies, our expert team covers all critical domains, including Quality Assurance (QA), Regulatory Affairs (RA), sterile and non-sterile manufacturing, and process engineering.
At DLS, we deliver comprehensive support encompassing R&D, regulatory submission, and commercial launch across a wide range of dosage forms, API processing, sterilization technologies, and global CDMO projects.
DLS is a dynamic, knowledge-driven Contract Research and Development Organization (CRDO) and Contract Manufacturing and Distribution Organization (CDMO) dedicated to advancing pharmaceutical innovation through a comprehensive suite of formulation development, analytical solutions, and cutting-edge manufacturing capabilities. We serve pharmaceutical manufacturing companies worldwide with a strong focus on quality, compliance, stable, safe, and effective drug products, as well as customer-centric innovation.
Our foundation is built upon decades of expertise through strategic partnerships and deep-rooted experience in pharmaceutical sciences, sophisticated instrumentation, and regulatory excellence. With state-of-the-art facilities certified by WHO-GMP, ISO 9001, and DSIR, DLS integrates science, technology, and a passion for innovation to deliver tailored solutions across the drug development lifecycle—from preclinical research to commercial manufacturing.
Our capabilities encompass a comprehensive range of services, including:
At the heart of Dosage Life Sciences Private Limited (DLS) is Dr. Rajesh K. Singh, a distinguished pharmaceutical leader with over the three decades of experience in steering Projects, innovation, strategy, and regulatory excellence across global markets.
Over the span of his career, Dr. Singh has held senior leadership positions at prominent pharmaceutical giants such as Ranbaxy Laboratories Limited, Glenmark Pharmaceuticals Limited, Alkem Laboratories Limited, and Morepen Laboratories Limited. In these roles, he successfully led multidisciplinary teams in the Operation, Projects (Green/Brown field), Infrastructure and process development, regulatory submission, and launch of over various drug products across domestic, regulated , semi-regulated & ROW markets.
Key Achievements:
Dr. Singh is highly regarded in the industry for his deep knowledge in Product/Process engineering, regulatory expertise, agile decision-making and unwavering commitment to quality and innovation.
A Vision for the Future
Under his leadership, DLS is set to become a Centre of Excellence in pharmaceutical consultancy, drug product and substance development, and ethical marketing. The company is committed to building a portfolio that reflects world-class standards, scientific precision, and customer-centric service and word class quality products in various segments.
“At DLS, we aim to bridge science with purpose — by developing high-quality, accessible pharmaceuticals and delivering them through trust, speed, and innovation.”
To become a leading and trusted name in the pharmaceutical industry by delivering innovative, affordable, and high-quality healthcare solutions that improve lives across the globe.
Our mission is to provide superior-quality medicines and services through continuous innovation, ethical business practices, and a strong commitment to customer satisfaction. We strive to build lasting partnerships and empower entrepreneurs through the best franchise opportunities and healthcare solutions.
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Our formulation portfolio will focus on high-demand therapeutic areas with a mix of generic and differentiated formulations. DLS’s product development will follow a science-driven, patient-centric approach, with a focus on bioavailability, stability, and regulatory compliance.
| Tablets – IR, ER, MR, ODTs |
| Capsules – Hard gelatine, Soft gelatine |
| Oral Liquids and Suspensions |
| Topical Preparations – Creams, Ointments, Gels |
| Injectables – Small volume parenteral (SVPs), Lyophilized vials |
| Sachets and Powders |
| Novel Drug Delivery Systems (NDDS) – Under development |
| Cardiovascular |
| Anti-Diabetic |
| Anti-Infective |
| Pain Management |
| Gastrointestinal |
| Dermatology |
| Respiratory |
| Neurology & Psychiatry |
| Vitamins & Nutraceuticals |
| Generic APIs aligned with key FDFs |
| Niche APIs with complex synthesis pathways |
| High-Potency APIs (HPAPIs) – Phase 2 |
| Intermediates and Custom Synthesis |
| In-house R&D-driven process development |
| Strong backward integration strategy |
| DMF preparation for global filings |
| Quality assurance in line with cGMP standards |
| Branded Generics – Promoted through medical representatives and specialty divisions |
| Institutional Business – Government tenders and hospital supplies |
| Trade Generics – PAN India distribution via stockists and retailers |
| Digital Healthcare Channels – E-commerce and telehealth platforms (Phase 2) |
| Therapeutic segment-focused divisions |
| Scientific-based promotional content |
| Continuous doctor engagement programs |
| Regional distribution networks with optimized logistics |
| Formulation development and tech transfer |
| API contract manufacturing |
| Dossier development and regulatory support |
| Technology transfer and lifecycle management |
Contact Us and Become a Partner.
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