Welcome To Kelly Pharmaceuticals

Kelly Pharmaceuticals is a Pharmaceutical company which can take care of complete Regulatory Affairs in a smooth and promising way. Kelly Pharmaceuticals is a team of certified pharmacists, experienced managers and a vibrant co-staff. It has been more than a decade that we are continually specialising our portfolio, easing out the way for hundreds of our clients and achieving enormous satisfaction for them.

Although we may be a regulatory company, but in no way we ignore the sciences behind your product. Kelly Pharmaceuticals has always believed that science should not be altered for coping with other challenges. And so, our team is specifically aligned towards keeping an eye on science of the drug along with the other duties. Our clientele is always ensured of the trueness of the work we begin.

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Who We Are

Kelly Pharmaceuticals is one of the India’s largest Pharmaceuticals organization responsible for manufacturing approximately 11-12 % of all drugs consumed in the different parts of country. The organization offers a comprehensive range of services starting from formulation development to market launch all en suite. Kelly Pharmaceuticals state of the art facilities are equipped to produce all modern dosage forms — tablets, capsules, liquid syrups and suspensions, injections, ointments, creams, gels, lotions, ayurveda and herbal preparations, nutraceutical and cosmetic preparations.

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Dedicated Team

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World Wide Service

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24/7 Supports


Custom Weighing and Packaging

Weighing scales and systems can help pharma manufacturing by monitoring incoming feedstock, controlling the production process and measuring production output for billing accuracy.


Technical Consulting and Support

With diverse and in-depth experience, our team of scientists and regulatory affairs specialists provide expert advice and services related to nonclinical safety testing, manufacturing.


Analytical Testing Services

Pharmaceutical analysis contract services can play an important role in your the development process and GMP manufacturing. Concerns about drug safety, costly development programs and complex manufacturing.


Contract Manufacturing and Services

We manufacture an extensive spectrum of branded pharmaceutical formulations in almost any form. Importers, distributors, and agents are always welcome to help us introduce our products.

Products For Every Need

We take utmost care to understand the needs of our customers. This enables us to develop innovative quality products at an affordable cost. Kelly Pharma has over 1000+ products being marketed and 200+ products under development and many more.


Research and Developement

DRUG PRODUCT DEVELOPMENT Kelly pharmaceutical Drug Product Development covers the entire process from concept to clinical and commercial manufacturing. Our Drug Product development starts with the screening of suitable formulations and processes to best meet the defined target product profile. These formulations / processes are analysed to identify the critical parameters potentially impacting the quality of the required defined target profile. Both formulations and processes are challenged and optimized to ensure that the Drug Product can be manufactured by a robust and efficient process according to QbD concepts. During scale-up critical parameters are established and verified with appropriate control strategies to ensure that quality attributes are consistently met for validation during routine manufacturing. Besides our dedication to quality we also focus on optimization of process ranges and robustness in order to improve manufacturing efficiency and reliability within a continuous improvement process.
Analytical Research and Development involves pre-formulation, stability and degradation studies on APIs and other drugs, and preparation of technical dossiers for registration in India and other countries. The Analytical Development team provides specific services to various departments of Mankind Research Centre. Kelly pharmaceutical provides method development and validation services for a wide range of analytical technologies. Compliance with both GLP and cGMP regulations enables the company to support all stages of pharmaceutical development in accordance with client-specific protocols, internal SOPs and FDA and ICH guidelines. The Analytical Development lab is equipped with HPLCs with PDA/UV detector, GC-FID with head space sampler, GC-HS-MS, UPLC, UPLC-MS, Ion chromatograph, Atomic-absorption Spectrophotometer, FTIR, UV-Vis Spectrophotometer, Total organic carbon analyser, NMR and XRD.
Pharmaceutical and Regulatory Services (PRSG) provides drug regulatory affairs (RA) solutions for products in the radiopharmaceutical, medicinal, veterinarian, cosmetics, and medical device industry. These services include support to prepare for a common technical document (CTD) or an electronic common technical document (eCTD), advice on the conduct of marketing authorisation applications, reviews and evaluations of documentation, and how to improve product lifecycles, as well as other strategic advice. The company’s highly qualified consultants provide its customers with expertise, which is tailored specifically to both their needs and regulatory and economic requirements.
The demand for drug discovery organizations to produce viable drug candidates is critical, as they try to progress pipelines in a pharmaceutical industry facing increased complexity and costs. A survey of drug discovery scientists was initiated. Respondents overwhelmingly point to project management practices as a valuable asset and offer several actionable suggestions.
A pilot plant can be used for  Evaluating the results of laboratory studies and making product and process corrections and improvements.  Producing small quantities of product for sensory, chemical, microbiological evaluations, limited market testing or furnishing samples to potential customers, shelf-life and storage stability studies.  Providing data that can be used in making a decision on whether or not to proceed to a full-scale production process; and in the case of a positive decision, designing and constructing a full-size plant or modifying an existing plant

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