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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
At R K Lifecare INC, We are a leading injectables manufacturer in India, dedicated to delivering high-quality pharmaceutical formulations. With state-of-the-art manufacturing facilities in Jhajjar, Haryana.
We specialize in producing a wide range of dry injectables including Cefazolin, Cefepime Hydrochloride, Cefoperazone Sodium, Cefotaxime, Ceftriaxone, and Cefuroxime. Our product portfolio includes Imipenem, Cilastatin, Ceftazidime, Tazobactam, Amoxicillin, Pantoprazole, Rabeprazole, Sulbactam, and more. and around the world pharmaceutical businesses in India standards, ensuring safe and effective formulations.
Our advanced R&D capabilities enable us to innovate and meet the emerging demands of the healthcare industry. With a strong distribution network and customer-centric approach, we serve hospitals, clinics, and manufacturing Committed to excellence, we follow strict quality control measures and global. Read More.
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
How do you ensure the safety of the raw materials used in your pharmaceuticals?
What quality standards do your pharmaceutical products adhere to?
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.
What is your process for handling product recalls, and how do you communicate with customers during such events?
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.
Does your company have sustainable practices in place for pharmaceutical manufacturing?
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.
How does your company stay compliant with changing regulations in the pharmaceutical industry?
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.
