logo
KCS notified as authorised body to inspect medical devices manufacturing facilities

KCS notified as authorised body to inspect medical devices manufacturing facilities

The Hindua day ago
The Central Drugs Standard Control Organisation (CDSCO), under the Ministry of Health and Family Welfare, has notified the Kalam Institute of Health Technology (KIHT) Certification Services (KCS) as the State's first regulatory body authorised to inspect the manufacturing facilities for Class A and Class B medical devices, according to a release here.
Among the 14 such notified bodies nationwide, KCS is the only one operational in Andhra Pradesh and Telangana, marking a milestone in the region's quality management capabilities.
Founded in July 2017, the KIHT, located on the AMTZ campus, is a Central government project supported by the Department of Biotechnology. It promotes and supports innovations in medical technologies through research and development, industry promotion, policy-making and knowledge repository.
Founded in April 2022, the KCS is accredited by the National Accreditation Board for Certification Bodies (NABCB).
The organisation offers comprehensive services, including ISO- 13485 certification, quality systems audit, risk management training, and CE‐mark consultancy — making it a full service hub for manufacturers seeking to meet global regulatory standards.
This approval brings immediate benefits to domestic manufacturers, particularly the MSMEs, by eliminating the need for audits outside the State — resulting in significant time and cost savings.
It also reinforces Andhra Pradesh's MedTech credentials, supporting national campaigns like 'Make in India' and 'ACI manufacturing', while making the region highly attractive for future investments.
This significant milestone empowers KCS to conduct independent regulatory audits for medical device manufacturers in accordance with the Medical Devices Rules (MDR)-2017 for Class A (low risk) and Class B (moderate risk), the release added, while underscoring the State's reputation as a business-friendly hub, ready to meet rising global demand in healthcare.
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Union Minister Pralhad Joshi seeks Siddaramaiah's apology after experts ruled out Covid jab caused heart attacks
Union Minister Pralhad Joshi seeks Siddaramaiah's apology after experts ruled out Covid jab caused heart attacks

Time of India

time12 hours ago

  • Time of India

Union Minister Pralhad Joshi seeks Siddaramaiah's apology after experts ruled out Covid jab caused heart attacks

Union Consumer Affairs & Renewable Energy Minister Pralhad Joshi on Sunday urged chief minister Siddaramaiah to apologise to scientists and researchers for 'insulting' them with his comments that Covid-19 vaccines may have caused heart attack deaths in Hassan district. Pralhad's demand came after an expert panel constituted by the state government into heart attack related deaths in Hassan district ruled out any link between the vaccination and heart attacks. When the pandemic broke out in the country, Prime Minister Narendra Modi acted swiftly and released grants. Siddaramaiah too took the shots of the vaccine in India, not overseas, Joshi told the media in Hubballi. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Depuratore d'acqua di nuova generazione: ecco quanto costa Depuratori d'acqua Scopri di più Undo The PM dealt with the pandemic far more effectively compared to other countries. But Siddaramaiah's statement was offensive to our scientists and questioned the efficacy of Indian vaccines where there was a huge demand for India-made pharma products in the oversea market, he said. Siddaramaiah's comments suggesting Covid-19 vaccination may have caused the recent heart-attack related deaths had triggered a wave of rebuttals from senior doctors, Biocon founder Kiran Mazumdar-Shaw and the BJP. Live Events The All-India Institute of Medical Sciences had dismissed any connection between the two. A study on the people who succumbed to sudden cardiac arrests did not reveal any link to the Covid vaccination, AIIMS experts said.

HC clarifies import rules for ayurvedic drugs in India
HC clarifies import rules for ayurvedic drugs in India

Time of India

timea day ago

  • Time of India

HC clarifies import rules for ayurvedic drugs in India

Cleared - mani Chennai: Madras high court has clarified that although no licence is required to import ayurvedic drugs into India, it is necessary that the imported products conform to the standards prescribed for similar products manufactured in India. Tired of too many ads? go ad free now "For such a purpose, it is necessary that such consignments be tested by one of the laboratories accredited to the Central Drugs Standard Control Organisation (CDSCO)," Justice Senthilkumar Ramamoorthy said. This process shall be overseen by the State Licensing Authority, which is the licensing authority for the manufacture of ayurvedic drugs. All expenses related to such testing shall be borne by the importer, the court stated. The court passed the order while disposing of a plea moved by Axeon Marketing India, the importer of 'Axe Brand Medicated Oil' from Singapore. They approached the court challenging the notices for alleged violation of the Drugs and Cosmetics Act. It argued that although the definition of "drug" read with the definition of ayurvedic, siddha, or unani drug indicates that the statute applies to ayurvedic drugs, the provisions related to the import of drugs are inapplicable to ayurvedic drugs. The import policy provides that the import of ayurvedic drugs may be undertaken "free", without a licence, the petitioner said. Opposing the contentions, the import commissionerate submitted that while the act and the rules deal with the manufacture of ayurvedic drugs in India and prescribe licensing requirements in relation thereto, licensing requirements have not been specifically prescribed for ayurvedic drugs. In the absence thereof, the import of ayurvedic drugs is prohibited. MSID:: 122269759 413 |

KCS notified as authorised body to inspect medical devices manufacturing facilities
KCS notified as authorised body to inspect medical devices manufacturing facilities

The Hindu

timea day ago

  • The Hindu

KCS notified as authorised body to inspect medical devices manufacturing facilities

The Central Drugs Standard Control Organisation (CDSCO), under the Ministry of Health and Family Welfare, has notified the Kalam Institute of Health Technology (KIHT) Certification Services (KCS) as the State's first regulatory body authorised to inspect the manufacturing facilities for Class A and Class B medical devices, according to a release here. Among the 14 such notified bodies nationwide, KCS is the only one operational in Andhra Pradesh and Telangana, marking a milestone in the region's quality management capabilities. Founded in July 2017, the KIHT, located on the AMTZ campus, is a Central government project supported by the Department of Biotechnology. It promotes and supports innovations in medical technologies through research and development, industry promotion, policy-making and knowledge repository. Founded in April 2022, the KCS is accredited by the National Accreditation Board for Certification Bodies (NABCB). The organisation offers comprehensive services, including ISO- 13485 certification, quality systems audit, risk management training, and CE‐mark consultancy — making it a full service hub for manufacturers seeking to meet global regulatory standards. This approval brings immediate benefits to domestic manufacturers, particularly the MSMEs, by eliminating the need for audits outside the State — resulting in significant time and cost savings. It also reinforces Andhra Pradesh's MedTech credentials, supporting national campaigns like 'Make in India' and 'ACI manufacturing', while making the region highly attractive for future investments. This significant milestone empowers KCS to conduct independent regulatory audits for medical device manufacturers in accordance with the Medical Devices Rules (MDR)-2017 for Class A (low risk) and Class B (moderate risk), the release added, while underscoring the State's reputation as a business-friendly hub, ready to meet rising global demand in healthcare.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store