- 01. ABOUT US
- 02. Founder
- 03. WHY US
- 04. VISION
- 05. MISSION
- 06. facilities
- 07. Our Services
- 08. Contact Us
Ananya Lifescience Private Limited was founded to fulfil the vision of Mr. Amar Lulla of a world class company that offers a comprehensive range of pharmaceuticals, biosimilars, nutraceuticals and OTC formulations to strategic partners in various markets.
These cutting edge formulations which have been developed through rigorous R&D, are designed for specific therapeutic categories and aim to address key concerns of patients and the medical fraternity.
Ananya Lifesciences is a professionally managed organization consisting of highly experienced professionals who are committed to provide solutions to the pharmaceutical industry, pharmaceutical research organizations, as well as nutraceutical, cosmetology and ayurceutical industries.
We add value through a comprehensive range of services including licensing of IP, product development and product lifecycle management, dossier preparation as well as turnkey site design and project execution for both national and international clients.
A key part of the L’Amar Groupe SA companies which have a presence in over 30 markets globally, Ananya Lifescience is the strong foundation which supports the group companies is establishing and sustaining the quality of the product portfolio and thereby ensuring significant brand equity.
Hon. Late Mr. Amar Lulla was born in 1948 and having qualified as a chartered accountant, he joined CIPLA in 1976.He was invited to the Board of Directors in 1990 and grew to become Cipla's Joint Managing Director & Chief Executive. His vision was to serve mankind with optimum health and wellness. To fulfil this vision, he worked with all schools of medicine, leading to development of highly effective products ranging from Allopathy to Ayurveda and Homeopathy. Out of this vision, Ananya Lifescience was formed in _, to bring to the world, healthcare solutions that combine with modern manufacturing techniques and delivery systems.
With a heritage of excellence and delivering quality work, we believe in long term partnerships that are based on trust and respect.
A single-minded focus on customer success.
A team that has strong domain knowledge offering their expertise in key areas critical for success in this industry.
To offer world class products, services and solutions to the pharma,biotech and nutraceutical industry across the globe.
To be a leading Innovative research and development organization in developing formulations, processes and technologies of any dosage form and make it commercially successful, whether it be for human or veterinary use.
To add value and be a true partner to pharmaceutical, OTC, Herbal and Nutraceutical companies. To develop IP in novel drug delivery and dosage forms. To formulate products to reach the market in a timely and cost-efficient manner delivering a wide product portfolio. To deliver patented formulations to the organizations who are engaged in high-end formulation research & Development. To develop technology-based products for pharma & allied field.
To reduce the long list of difficult to formulate product by employing the right strategy & technology with scientific manpower.
To support healthcare industry and our country by patenting our plants and parts inherited by us from our ancestors by carrying out in-depth research in natural /traditional system of medicine in a modernized systematic manner to tackle life threatening diseases.
To offer world class products, services and solutions to the pharma, biotech and nutraceutical industry across the globe.
To be a leading Innovative research and development organization in developing formulations, processes and technologies of any dosage form and make it commercially successful, whether it be for human or veterinary use.
We have a dedicated facility located in India for product development and commercial manufacture. Our facility supports the study for almost all scale-up & engineering variables. We have adequate scientific manpower, equipment and instruments which can cater the formulation development as well as scale-up studies that can be done by QBD approach. Our facility supports batch sizes starting from 200gm to 250kg. The GMP area is used for manufacturing the batches for pilot BE studies, clinical studies and commercial batches.
Our GMP facility in Goa manufactures OSD, liquids, and topicals formulated using phyto extracts.
Our new facility will be launched in 2025 which is planned as a world class facility that will manufacture Oral solids, Liquids, and Granules. This facility will also have a production line for Mouth Dissolving Oral Films.
* Partnerships Through JVs
* Sales, Marketing and Distribution Services
* Marketing Through OTC / Ethical Channel
* Distribution across UAE and India
Connecting Businesses through Strategic ‘Win Win’ Models.
a. Oral Mouth Dissolving Films
Our patented Oral Film Product range comprises of 10 Pharma formulations and 20 OTC/Nutra formulations.
b. Biologics
We have developed a strong portfolio of Biologics with 2 ready for commercial launch in 2024 and the remaining in the pipeline which will be commercialized in 2026.
Product Development
We provide an end to end solution in product development & product life cycle management. Our expertise is in product development, pharmaceutical process development by non-infringing route and technology development. We have successfully carried out product development for regulated markets, notably for USA market, in pharma, food & other allied fields of healthcare segment.
Formulation Development
Any dosage form, from any source of Medicine like Synthetic, Herbal, Nutraceuticals, Cosmetic preparations Oral Solid Dose Oral Solid dosage form like tablet, granules, capsules, dry syrups.
⦿ Liquid Dosage Forms
⦿ Parenteral Formulations
⦿ Ointments and Creams
Analytical Method Development
We carry out both analytical method development and method validation of our products. We also take projects for either method validation or both development and validation.
Stability Study Area
We have a dedicated area for shelf-life study of the products. We carry out the Stability Study as per ICH guideline.
⦿ Scale up & Registration Batches
⦿ Commercial Production
⦿ Sourcing APIs
⦿ Formulations and IP
Technical Services
⦿ Site Design and End to End Project Execution
⦿ Project Management
⦿ GMP & Quality Assurance
⦿ Regulatory Affairs
⦿ Scientific Services
⦿ Clinical Trials
Legal Support
⦿ Contract Drafting
➜ Formulation Development
➜ Technology Transfer
➜ Distribution
➜ Licensing & Supply
➜ Contract Manufacturing
Human Resource
