We source our raw materials from reputable suppliers who meet stringent quality criteria. Our dedicated procurement team conducts thorough inspections and audits to guarantee that the raw materials comply with our quality standards before they are incorporated into our manufacturing processes.
Human Dry Injection

Human dry injection manufacturing involves sterile powder manufacturing, vial filling, lyophilization, quality control, and packaging for medical use.
Click HereVeterinary Dry Injections

Veterinary dry injection manufacturing involves the production of sterile, powder-based injectable medications for animal healthcare.
Click HereInjection Manufacturing

Injection manufacturing involves the manufacturing, sterilization,
and packaging of liquid or dry medications for medical use.
Click HereThird Party Manufacturing

Third-party manufacturing allows companies to outsource production to specialty manufacturers for cost-effective.
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Pharmaceutical Manufacturer and Exporter Company in Delhi, India
R K Lifecare INC is One of the Fast-Emerging Dry Injection Manufacturers in India. Headquartered in the Heart of the Country New Delhi, the Company Has a State-Of-The-Art Research and Manufacturing Facility in Jhajjar, Haryana.
There Is a Dedicated Team of Researchers and Scientists Working on the Development of Standard-Quality Dry Injection Powders, Liquid Injections and Veterinary Injections.
The Company Has Earned a Reputation for Providing High-Quality, Effective and Competitive Medication Solutions for Both Human and Veterinary Uses.
We, R K Lifecare Inc, Specialize in Developing Innovative Formulations Improving Our Medical Services and Pushing Qualitative Upgradation in Dry Injections by Integrating All the Required Expertise and Machinery at the Research and Manufacturing Sites.

Process of Making Dry Injection
The process of making dry injections involves blending active pharmaceutical ingredients (API) with excipients, followed by sterile filtration. The mixture is then lyophilized (freeze-dried) to remove moisture, ensuring stability. The sterile powder is filled into vials under aseptic conditions and sealed, ready for reconstitution before use.
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Frequently Ask Questions
Our pharmaceutical products adhere to the highest quality standards set by regulatory authorities such as the FDA and EMA. We implement rigorous quality control measures at every stage of the manufacturing process to ensure the safety, purity, and efficacy of our products.
In the unlikely event of a product recall, we have a well-established recall protocol in place. Our priority is customer safety, and we promptly communicate recall information through various channels, including our website, direct customer notifications, and collaboration with regulatory authorities.
Given the dynamic nature of the pharmaceutical industry, customers want assurance that the company is proactive in staying abreast of regulatory changes. This question highlights the company's commitment to compliance and its ability to adapt to evolving industry standards.
We have a dedicated regulatory affairs team that closely monitors changes in pharmaceutical regulations globally. Regular training sessions and continuous education ensure that our staff is well-informed and able to adapt swiftly to evolving standards. This commitment allows us to maintain compliance and uphold the highest industry benchmarks.