Here is the List of 2019 approved drugs in India; read the blog to know all the details related to drug approvals in India. S.No Name of drug Indication Date of issue 1 Fenspiride hydrochloride film coated extended release tablet 80 mg and Fenspiride hydrochloride
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To know all the details about the 2020 approved drugs in india, read this blog and check all the details that are mentioned below:- S.No Name of drug Indication Date of issue 1 Cidofovir dihydrate bulk drug and Cidofovir injection 75 mg/ ml (5 ml
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If you are curious to know the year 2021 approved drugs in India, here is the list of approved drugs list by the Central Drug Standard Control Organization, widely known as CDSCO. CDSCO is the Government of India’s Ministry that maintains Health and Family Welfare.
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If you want to know what are the year 2022 approved drugs in india, then here is your go-to solution, as all the approved drug in the year 2022 is mentioned in the list given below. Also, all other details are provided after the table.
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The list of the 2023 approved drugs in India is mentioned below. To know the name of the drugs and indication of the medicine, their date of issuance is also listed under the given table. Check out the Q & A as it covers all
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If you are confused and want to check the list of approved drugs in India, then here is The proper list of the approved drugs. This article consists of details like how to register medicines in India, what the requirements for drug registration are in
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So, if you are struggling with this confusion about what a Clinical Evaluation Report is, then here is your answer. The Clinical Evaluation Report is a technical document in the form of a document; this Clinical Evaluation Report consists of an analysis of the medical
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Medical Device Reporting (MDR) plays a crucial role in ensuring the safety and effectiveness of medical devices in healthcare settings. Enforced by regulatory agencies such as the FDA, MDR mandates the reporting of adverse events, product issues, and malfunctions associated with medical devices. This regulatory
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If you are confused and searching for the answer of what Investigational Device Exemption is, so basically is widely known as an “IDE,” here is your answer. In simple terms, The IDE is a Regulatory Submission that works as a permit for the investigational device
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Ensuring the safety and efficacy of medical devices is crucial for protecting patients and meeting regulatory standards. A Risk Management File plays a central role in this process. It is a comprehensive document that records all activities related to identifying, evaluating, and controlling risks associated
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