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HOME CLIENTS FACTS CONTACT ABOUT US SERVICES HOME REGULTORY CONSULTANCY FOR CDSCO WITH 20+ YEARS OF EXPERIENCE PHARMA AND MEDICAL DEVICE REGULATORY CONSULTANCY SERVICES FOR INDIA MARKET Connect with us Medical Device Licenses We are providing end-to-end regulatory services for Medical Device importers, manufacturers and supplies. Our team is experienced for swift regulatory submissions and approvals. Know more PHARMA (DCGI) NEW DRUGS CT NOCs MFG. APPROVALS COSMETICS IMPORT REGISTRATION MFG. APPROVALS FOOD & NUTRACEUTICAL PRODUCTS (FSSAI APPROVALS) MEDICAL DEVICES & VACCINES MD14, MD5, MD26 and More SERVICES OUR SERVICES Create a regulatory strategy There are numerous ways to proceed for each kind of product. Our technical team will study your products upon which we will create a route best fitted for getting approvals of products from Indian Authorities. Our team will predict possible challenges and create a strategy to overcome them. Pre-screening of documents Information presented rightly accelerates the timeline and reduces complexities. Our experienced technical team audits each document for any errors, updations or information that is necessary for India’s updated norms, validating them with recent changes or authoritative texts. Timeline Management We will make sure that everything keeps moving and fetch results under best timelines. A project coordinator from our company will collaborate with your team to assist you over the documents and perform regular follow-ups — a culture that has been valued by most of our clients. On-demand Services En-route there are several other services which we offer as the need comes. Our team can handle your CDSCO Correspondences, prepare justification rationales, research and format replies to queries, market insights, networking, online and offline submissions, PV Services, general assistance and more. AREA OF SERVICES NEW DRUG APPROVALS FDC APPROVALS IMPORT & REGISTRATION GLOBAL CLINICAL TRIALS BA/BE NOC VACCINES/ BIOTECH PRODUCTS COSMETICS' IMPORT REGISTRATION MEDICAL DEVICE IMPORT REGISTRATION NUTRACEUTICALS/FOOD SUPPLEMENTS APPROVAL - FSSAI ETHICS COMMITTEE REGISTRATION WHO WE ARE Rihim Pharma Consultancy is an extension of any Pharmaceutical company which can take care of complete Regulatory Affairs in a smooth and promising way. Rihim Pharma 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. Rihim Pharma 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. ​ An ISO 9001:2015 Certified Company ABOUT US CLIENTS OUR CLIENTS We have always been there as a part of our clients' own division. We have enjoyed working with a more than 300 Pharma giants and have succeeded to serve efficiently. Here are some of our long-time and popular clients... Amgen Logo-Menarini_CS takeda-shire-7x4 Logo_of_PT_Bio_Farma_(Persero) 5856a7bb4f6ae202fedf276b Dabur_Logo.svg logo Advanced-Hair-Studio-in-Ahmedabad 003-APTOS-new fresenius Logo shah distributers LAMBDA_LOGO_png veeda logo logo-2 granules India logo.jpg 103575-rb naprod ALKEM Signet Screen Shot 2018-08-27 at 12.35.30 PM logo-1 umicore logo_15 ambeal Screen Shot 2018-08-27 at 12.40.21 PM default Screen Shot 2016-01-26 at 11.05.32 PM innova-logo logo-1 118_RIVPRA_FORMULATION_PVT.LTD EuMUIbuVkAQwBMA omron logo 1573755321274 1519864698368 FACTS 8500+ SUBMISSIONS 500+ CLIENTS 100% SUCCESSFUL APPORVALS FACTS CONTACT Send us your enquiry First Name Last Name Email Company Write a message Submit Lets work together. Brief us about your requirements. 518-519, Ring Road Mall Rohini Sector-3 New Delhi, India - 110085 info@rihimpharma.com 011-47564040 or +91-9891072226

20 Years of Expertise in CDSCO Services and Medical Device Registration At Rihim Pharma Consultancy, we understand the unique challenges and requirements of medical device registrations, and we have the knowledge, 2 decades of expertise, and key resources to guide you through the entire process. We take pride in our commitment to providing personalized, tailored services that meet the specific needs of our 500+ clients. Connect with us Services | The Rihim Difference | Contact | About the Founder Our Clients Complex Medical Device Regulations make registrations more Expensive Despite a high-potential market, medical device registration in India can be a complex and time-consuming process for importers, traders, manufacturers and MNCs alike; presenting significant challenges for companies seeking to enter the Indian market. The regulatory landscape in India is constantly evolving, and we help you to simplify and smoothen your India regulatory strategy. Get a complimentary quote Subscribe to Rihim's monthly emails Send enquiry Our Services Import License or Registration of Medical Devices (MD 14) » Manufacturing License (MD 5) » Registration of an Innovative/New Medical Device (MD 26) Post approval changes ISO 13485 from DCGI’s notified agencies » Clinical Trial Approvals » Import Test License (MD 16) » In-Vitro Diagnostic Products/Kits » Services - Medical Device What makes us different? Let’s count. Rihim Difference - MD 3-Layer Review of every Medical Device Applicati o n One way we demonstrate this commitment is by having each project reviewed by three layers of internal experts. This ensures that every project is completed with the utmost attention to detail, reducing post-submission errors or queries, and maximising your chances of approval. Our approval process exceeds the industry standard in terms of speed. In addition, our efficient approvals are well known throughout the industry. We understand that time is money, and we work tirelessly to ensure that our clients’ products are approved as quickly as possible, without compromising on quality or regulatory compliance. Dedicated Success Team for each Project We further demonstrate our commitment to providing exceptional service by dedicating a project management team to each client. This ensures that every project is completed on time and with the utmost attention to detail. Our project management team works closely with our clients to understand their unique needs and goals, and they provide regular updates on progress throughout the registration process. Specialised for CDSCO Finally, our strong followup with regulatory bodies are unrivalled in the industry. This helps us stay updated with every-day regulatory changes in requirements, address complicated queries and achieve timely approvals. Let’s make a good team So why choose Rihim for your medical device registration needs in CDSCO, India? We offer unparalleled expertise, personalized service, timely approvals, and a proven track record of success with 8500+ approvals from CDSCO. Our team is dedicated to helping you achieve your goals and ensuring that your products reach the Indian market as quickly and smoothly as possible, in compliance with all the applicable regulations. ​ To learn more about our services and how we can help you with your medical device registration needs, please contact us today. We look forward to working with you! Email: info@rihimpharma.com Call or WhatsApp: +91-9891072226 Office: 518-520, Ring Road Mall Mangalam Place, Rohini Sec-3 New Delhi 110085, India Ph: +91-11-47564040 Get a complimentary quote Subscribe to Rihim's monthly emails Send enquiry Contact - Medical Device About our Founder & CEO Meet Mr. Nilesh Thosani, the founder of Rihim Pharma Consultancy. With over 20 years of experience in the pharma, medical device, vaccines, biotechnology and related industries, he has established himself as one of the foremost experts in regulatory affairs in India. Mr. Thosani is a trailblazer in the industry, having established the first regulatory consulting company in India to work with the Central Drugs Standard Control Organization (CDSCO). He has played a key role in shaping the regulatory landscape in India and has helped numerous companies successfully navigate the complex and ever-changing regulatory requirements. ​ Over the years, Mr. Thosani has earned numerous accolades for his exceptional work, including awards from companies such as Akzo Nobel for being the best service provider. His commitment to providing win-win solutions for all stakeholders has earned him a reputation as a trusted and reliable partner in the industry. ​ In addition to his extensive industry experience, Mr. Thosani has developed positive relationships with regulatory authorities and the Ministry of Health in India. These relationships, combined with his deep knowledge of the regulatory landscape, have made him an invaluable resource for companies seeking to enter the Indian market. ​ As a go-getter and inspiring leader, Mr. Thosani is dedicated to providing exceptional service to his clients and helping them achieve their goals. He leads by example, instilling a culture of excellence and accountability throughout the organization. His passion for the industry and commitment to success make him a true asset to the Rihim Pharma Consultancy team. Nilesh Thosani nilesh@rihimpharma.com About the Founder

Privacy Policy Introduction ​ Welcome to Rihim Pharma Consultancy! We are committed to protecting your privacy and ensuring the security of your personal information. This Privacy Policy outlines how we collect, use, and safeguard your data when you interact with our services. ​ Information We Collect ​ Personal Information: We may collect personal information such as your name, contact details, and professional background when you engage with our services. Usage Data: We gather information about how you use our website, including IP addresses, browser type, and pages visited. This will help us improve our services and enhance your experience. ​ How We Use Your Information ​ Service Delivery: We use your personal information to provide our consultancy services, respond to inquiries, and manage client relationships. Communication: We may contact you via email or phone to share updates, newsletters, or relevant information related to our services. Analytics: We analyze usage data to understand user behavior, improve our website, and tailor our offerings to your needs. ​ Data Security ​ We take data security seriously. We implement industry-standard measures to protect your information from unauthorized access, disclosure, or alteration. ​ Cookies and Tracking Technologies ​ Our website uses cookies to enhance your browsing experience. You can adjust your browser settings to manage cookies or opt out of tracking. ​ Third-Party Links ​ Our website may contain links to third-party sites. Please review their privacy policies, as we are not responsible for their practices. ​ Your Rights ​ You have the right to access, update, or delete your personal information. If you have any requests or concerns, please contact us using the details below. ​ Contact Us ​ If you have any questions or need further clarification, feel free to reach out to us: ​ Email: info@rihimpharma.com Phone: +91-11-47564040

WORK FOR QUALITY REGULATORY PROFESSIONAL M. PHARMA (DRA) Undertake regulatory submissions to DCGI Compilation of application as per checklists Coordinate with clients to resolve their queries and follow-up for on-going projects Able to communicate with new leads and thrive to materialise them Team up with technical experts in the office and solve challenges regarding Regulatory Affairs Package: 3 Lakhs p.a. (1-2 Years Experience) 1.80 Lakhs p.a. (Fresher) Apply now

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