Regulatory Affairs
Our Regulatory Affairs department has competency in handling multiple regulatory activities from clinical trial applications.
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Right studies at the right time using proven experimental design, quality compliant management systems, experienced professionals, and state-of-the-art facilities with current technologies
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We understand the standard operating procedures and regional operational requirements to facilitate Phase I to IV clinical trials including proof of concept study. We are experienced in managing clinical trials of varied sizes and complexity in different therapeutic areas
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We ensure that your projects will receive the highest level of quality by implementing Quality Management Systems by understanding the need for required compliance as per regulatory requirements.
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Our team remains involved at every stage of data management and works closely with study sites to generate clean datasets with total quality.
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Visitors
A well organised international self-regulating management service Centre, Innayat, establishes in the year 2020. With the headquarters in Haryana, it sprouts rapidly in Malaysia, Bangalore, & Gurgaon. Around the world, it lends its service to the clients who claim the services in Medical Devices industries, Pharmaceuticals, Nutraceuticals, Herbs, & in Cosmetics excessively. With at most prompt time and quality, it heals the requirements of pharmaceutical companies to transform their ideas and concepts into a successful product with efficient drug development. Our innovative approaches to the clients’ needs make us unique among the CROs.
Our Clinical Operations team is experienced in managing clinical trials of varied sizes and complexity in different therapeutic areas like Infectious Diseases, Oncology, Cardiology, Gastroenterology, Nephrology, Diabetes, Obstetrics & Gynaecology, Urology, Pain Management, Dermatology, Ophthalmology, Neurology, Psychiatry, and Parenteral nutrition. Our team has executed many NDA, ANDA, and Biosimilar products clinical development programs including vaccines. The team comprises people with the right attitude, flexibility, reliability, and commitment to excellence.
Our Regulatory Affairs department has competency in handling multiple regulatory activities from clinical trial applications.
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Our data management team can manage multi-center, multi-country studies in both electronic and paper based format.
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INNYATCRO provides critical preclinical research data and innovative solutions through the conduct of the right studies.
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Faster you reach each milestone, the faster your compound can be advanced to the next stage.
We are passionate and determined about what we do and want our name to stand for Excellence.
We build long lasting, collaborate relationships with our customers and work with them as partners.
We value the importance of time and adhere to our commitments.