Procedure for submission of cough syrups for Testing

Mandatory Testing of Cough Syrup before ExportProcedure for submission of cough syrups for Testing

Cough syrup exporters will have to undertake testing of their products at specified Government Laboratories and obtain Production of Certificate of Analysis with effect from June 1 before getting permission for the outbound shipments

Ministry of Commerce & Industry has issued a Notification No.06/2023 dated 22nd May 2023 permiting export of cough syrups, subject to the export sample being tested and production of Certificate of Analysis (COA) issued by any of the Central Government Laboratories and any NABL Accredited State Drug Testing Laboratory.

The specified Central Government labs include Indian Pharmacopoeia Commission, Regional Drug Testing Lab (RDTL – Chandigarh), Central Drugs Lab (CDL – Kolkata), Central Drug Testing Lab (CDTL – Chennai Hyderabad, Mumbai), RDTL (Guwahati)] and the NABL (National Accreditation Board for Testing and Calibration Laboratories) accredited drug testing labs of State Governments

In order to facilitate the process of testing of cough syrups at the said laboratories, the following are the pre-requisite requirements for submission of samples :

  1. Covering letter from the Manufacturer / Exporter on Letterhead addressed to concerned Laboratory
  2. Manufacturing License of the product for Export purpose
  3. Export Order
  4. Representative sample from the export consignment
  5. Thrice the quantity required for performing complete analysis of the sample
  6. Qualitative composition of product including excipients
  7. Certificate of analysis by the manufacturer of the particular batch and method of analysis (STP)
  8. Reference / Working standard (with traceability certificate) and placebo as applicable

Source: https://www.dgft.gov.in/CP/?opt=notification

EGA 2023 – Application Now Open

Envirocare Green Awards 2023

Envirocare Green Awards is an initiative by Envirocare Labs started in 2018 with a vision to motivate and empower professionals & organization’s in the field of environment. 

EGA is a non-commercial activity of self-motivated and like-minded people dedicated to making a positive difference to Sustainable Care. 

The objective is to inspire stakeholders to think green & contribute towards a world that is not only progressive but also responsible towards its provider.

The applicants for these awards will be evaluated by an independent international Jury – renowned & respected in their professional fields. The award ceremony would be preceded by keynote speaker sessions.  

The application for this award is online and is open for across the globe under the following categories:

1. Individual / s

2. Private Ltd / LLP / MSME

3. Public Sector / Large Corporates

4. Non Government Organisation NGO / Cooperatives

5. Government Organisation / Municipal

6. Academia

7. Others

To apply please click here for online Google Form:https://forms.gle/ZfWBjSR8PA6W5Bqe7

The short listed applicants will be required to make online presentation for Jury evaluation. The data submitted would be confidential and used only for the purpose of EGA

Application deadline 15th June 2023, Please feel free to reach out to EGA Secretariat Ms Deenal Shah: +91 9167232025 | ega@envirocare.co.in

For regular updates on EGA 2023 , visit  https://lnkd.in/eDiKu3R

Best Practices in Social Sector

NITI Aayog released the “Best Practices in Social Sector: A Compendium, 2023”

NITI Aayog released the “Best Practices in Social Sector: A Compendium, 2023” in collaboration with the United Nations Development Programme.

To commemorate 75 years of India’s independence and highlight and laud the efforts of Union Ministries and State Governments, this compendium includes 75 case studies cutting across 14 key social sectors. The case studies have been sourced from all States/ Union Territories and 30 Ministries and Departments of the Government of India.

The seventy-five best practices highlight models which are innovative, sustainable, replicable and impactful. The aim of this exercise has been to synthesise lessons for the future to expand, enhance and improve life at the grassroots level. Due care was taken to ensure that the cases identified are spread over diverse themes, including education, health and nutrition, e-governance and digitization, agriculture, women’s empowerment, sports, and financial inclusion, among others.

Source: https://niti.gov.in/node/3568

Guidelines – AMD-CF Scheme

Govt releases Guidelines for scheme for Assistance to Medical Devices Clusters

The Department of Pharmaceuticals (DoP) has come out with the guidelines for the scheme for Assistance to Medical Device Clusters for Common Facilities (AMD-CF) with proposed financial outlay of Rs. 300 crore to offer financial assistance to strengthen the existing and new medical device clusters through creation of common infrastructure facilities

The Scheme, with two sub-schemes, is expected to help in boosting the domestic manufacturing capacity and improving the quality of clusters for sustainable growth of the medical devices sector.

The scheme further intends to support central or state governments, institutions, or organisations to establish or strengthen the testing laboratories for medical devices to meet the needs arising due to the roll out of the licensing regime of the Medical Devices Rules (MDR), 2017.

The Scheme has two components or sub schemes – Assistance for Common Facilities (CF) and Assistance for Testing Facilities (TF) – and would be running for three years from 2023-24 to 2025-26. The tenure of the scheme is from the financial year 2023-24 to the financial year 2026-27.

Both the sub-schemes are designed to set up 12 common facilities and 12 testing laboratories, under which the common facilities will be supported with a financial assistance of Rs. 240 crore (Rs. 48 crore in the first year, Rs. 128 crore in the second and Rs 64 crore in the third year) for the common facilities and Rs. 60 crore (Rs. 18 crore for the first, Rs. 30 crore for the second and Rs. 12 crore for the third year) for the testing facilities.

Assistance for Common Facilities is planned to strengthen the medical devices clusters’ capacity for their sustained growth by creating common infrastructure facilities.

Medical devices manufacturing units in a cluster who have come together to form a Special Purpose Vehicle (SPV) to execute the project of developing common facilities and the clusters promoted by the State governments, are expected to benefit from the sub-scheme.

There shall be a minimum of five medical device manufacturing units as members of SPV. Clusters promoted by state governments may not need to form an SPV.

The SPV should have representatives from cluster members, financial institutions, state and central government and R&D organisations and the individual manufacturing unit cannot hold more than 40 per cent in the SPV. The Medical Devices enterprises shall hold at least 51 per cent equity of the SPV.

For Common Infrastructure Facilities for medical device clusters, the limit of support will be 70 per cent of the approved project cost or Rs. 20 crore, whichever is less, as per the approval of the Scheme Steering Committee (SSC).

The sub scheme is expected to have benefits including improvement in quality of medical devices, regulatory compliance specified for medical devices, increased availability of trained personnel for the clusters, increased competitiveness of units in the cluster and reduction in the manufacturing cost of the devices.

The sub scheme on assistance for Testing Facilities is aimed at strengthening availability of more Medical Device Testing Laboratories in order to boost manufacturing of quality medical devices, and national or state level government of private institutions interested to establish or strengthen testing facilities for medical devices to test Class A, B, C and D medical devices including in vitro diagnostic medical devices under MDR, 2017 can apply for the assistance.

The guideline proposes a Technical Committee constituted by the DoP to assist the SSC, which will have one representative each from the Central Drugs Standard Control Organisation (CDSCO), industry and academia, and ICMR, and two representative experts having knowledge and experience in the process development, R&D, product design, testing of medical devices or medical devices manufacturing from relevant institutes such as NIPER, IISc, IITs, Sree Chitra Thirunal Institute of Medical Sciences and Technology, and CSIR, among others.

The DoP will provide overall policy, coordination and management support for the implementation of the Scheme, while the proposals under the scheme will be considered for approval by the SSC, which will be headed by the Secretary of DoP as the Chairperson, and will have members including the Drugs Controller General of India, Financial Advisor of DoP, Joint Secretary (Schemes and Medical Devices), DoP, representatives of the Ministry of Micro, Small and Medium Enterprises (MSME), the Ministry of Electronics and Information Technology (MeitY), the Department for Promotion of Industry and Internal Trade (DPIIT), and the director or the deputy secretary (Schemes) of the DoP.

Source: https://thehealthmaster.com/2023/05/11/govt-releases-guidelines-for-scheme-for-assistance-to-medical-devices-clusters/

Industry Update

Centre Notifies National Medical Device Policy 2023

The Union government on 27th April 2023 notified the National Medical Device Policy 2023, aiming to establish India as a global leader in manufacturing and innovation of medical devices by achieving a 10-12% share in the expanding global market over the next 25 years.

It outlines a regulatory mechanism, protocol for setting up standards for medical devices, price control, research and development (R&D), and a code of ethics for industry associations to ensure the ethical marketing of medical devices

According to the notification, the policy will guarantee access to patent-centric, innovative, and affordable healthcare products of exceptional quality for improved healthcare outcomes. It seeks to facilitate the growth of the medical devices sector to cater to both the Indian and global markets while promoting safety and quality. The policy provides a roadmap for the accelerated growth of the medical devices sector.

The policy plans to promote innovation and R&D, including joint R&D projects involving academic institutions and industry under the proposed ‘National Policy on R&D and Innovation in the Pharma-MedTech Sector in India’. This approach fosters collaboration between academic institutions and the medical devices industry.

Furthermore, the policy seeks to attract investments in the sector, adding to existing schemes and interventions to promote indigenous manufacturing, build competitiveness, and develop an ecosystem for manufacturing.

Source:https://www.livemint.com/

https://pharmaceuticals.gov.in/policy/national-medical-device-policy-2023

Industry Update

Plastic Waste Management (Amendment) Rules, 2023

The Ministry of Environment, Forest and Climate Change of India has published a notification in the Gazette of India announcing the Plastic Waste Management (Amendment) Rules, 2023. The Rules came into force on the day of publication in the Gazette and are an amendment to the Plastic Waste Management Rules, 2016 previously amended by the Plastic Waste Management (Second Amendment) Rules, 2022.

In rule 10, which states “Protocols for compostable plastic material” in the sub- rule (5), in the provision, for the figures “2023” occurring at both places, the figures “2024” shall respectively be substituted.

In Rule 11 which states “Marking or Labeling” in sub-rule (1), in clause (a), after sub-clause (iii)  the following clause shall be inserted, namely:-   “ for rigid plastic packaging “

In Rule 13,-

  • in sub-rule (2), the words “or for renewal of registration” shall be omitted;
  • for sub-rule (9), the following sub-rule shall be substituted, namely :-
    • “9(a) The registration granted under this rule shall be changed only on the request of Producers, Importers & Brand owners, under the existing Extended Producer Responsibility registration ,
    • (b) The registration granted under this rule shall be valid for a period of one year, unless revoked, suspended or cancelled and shall subsequently be granted for three years.”

In Schedule II, Paragraph in paragraph 6 for clause (6.6), the following clause shall be substituted, namely :-

While registering, the entities shall have to provide PAN Number, GST Number, CIN Number in case of company, and the entities may provide Aadhar Number, and shall provide PAN Number of authorized person or representative and any other necessary information as required

The last date for the filing of annual returns is 31st October 2023 (for producers, importers and brand owners of plastic packaging) and 31st July 2023 (for plastic waste processors, recyclers and other waste processors including industrial composting facilities) for the financial year 2022-2023

Industry Update

Relaxation of procurement of certain Medical Equipments and Drugs through Global Tender Enquiry

Government of India, Department of Expenditure,Procurement Policy Division has given exemptions for certain Medical equipment’s and drugs from the instructions related to GTEs (Global Tender Enquiry)  issued by this department on 15.2.2020

On the request of Ministry of Health and Family Welfare (MoH&FW)  on 22.3.2023, these exemptions are being extended for one year i.e till 31.03.2024 or further orders, whichever is earlier.

Exemptions will only be available for 364 Medical Devices ( as given in Annexure A) and 70 Drugs ( Annexure B)

Source: https://doe.gov.in/procurement-policy-division-0

Launch of Healthcare textiles processing facility certification Scheme

Healthcare Textiles Processing Facility Certification Scheme Launched in India

On the occasion of World Health Day on 7 April, the triple A partnership of AMTZ LTD, Association of Healthcare Providers – AHPI (India) and Association of Indian Medical Device Industry – Aimed India, launched Healthcare Textiles Processing Facility Certification Scheme (HTPFCS) to ensure the quality of healthcare textiles, including personal protective equipment (PPE), by certifying the facilities or laundries that process them for reuse

While the Covid-19 pandemic has highlighted the importance of healthcare textiles and PPE in protecting healthcare workers and patients from infection, the quality of these products depends not only on the materials used but also on the processing facilities where they are sterilized, cleaned, and packaged.

The Healthcare Textiles Processing Facility Certification Scheme will help ensure that these facilities meet international standards for quality and safety. It aligns with international standards and guidelines, including those of the World Health Organization (WHO) and the International Organization for Standardization (ISO).

Under the scheme, healthcare textiles processing facilities can apply for certification by undergoing a rigorous evaluation process that includes site visits, documentation reviews, and testing of samples.The certification will be valid for three years, after which the facility will need to undergo a recertification process.

The Certification would be carried out by independent third party certifying agencies to be accredited as per applicable international standard, ISO 17065, and approved by AMTZ to assure their competence, impartiality and consistent implementation of certification process.

The Healthcare Textiles Processing Facility Certification Scheme is open for applications from healthcare textiles processing facilities in India and abroad.

source:http://www.pharmabiz.com/NewsDetails.aspx?aid=157437&sid=1#:~:text=The%20Healthcare%20Textiles%20Processing%20Facility%20Certification%20Scheme%20is%20a%20welcome,of%20healthcare%20textiles%20and%20PPE.

Conference on Telehealth

SMART Hospitals India Conference 2023 at Medical Fair India, Pragati Maidan, New Delhi

SMART Hospitals India Conference 2023 at Medical Fair India, New Delhi

Conference Theme 2023

Telehealth : Where SMART Technologies connect with healthcare settings for better patient outcomes

Healthcare Service Providers are increasingly adopting multiple digital health initiatives for better patient connect and seamless delivery of patient care. FUTURE SMART Healthcare Establishments focus on providing solutions to meet the rising needs of SMART PATIENTS across the globe.

Smart Hospitals Business Sessions this year are designed to create focused discussions around TELEHEALTH Technologies as listed below

Session 1 – Telehealth Technologies , Solutions for Better Patient Care in Healthcare Settings in India

Session 2 – Delivering Quality Care through Telehealth Quality System Program in Clinical Settings

Session 3 – Health Technology Assessments and Regulatory Requirements of Telehealth Solutions in India

Program Date :

Date: 29th April 2023 – Saturday
Time: 10:00 a.m. – 5:00 p.m.
Venue: Hall 5, Pragati Maidan, New Delhi

For more information on program, registration links, do visit – https://www.medicalfair-india.com/en/Special_Shows/Smart_Hospitals

Prior registration is a must to attend the conference.

For enquiries related to Conference Partnerships, Stall bookings in the Expo, enquiries, 𝗽𝗹𝘀 𝘄𝗿𝗶𝘁𝗲 𝘁𝗼 :

VermaA@md-india.com / +91-124-4544507


For enquiries related to Delegate Registration to the Conference, please write to :

Ms Rama Venugopal
Vice Chairperson – SMART Hospitals Conference
Email – info@smarthospitals.events
WhatsApp – +91 7338992778 / +91 9840870532

IAF CertSearch

IAF CertSearch Team Identifies 20,000 Fake or Fraudulent ISO QMS Certs

As of 2023, more than 27,000 medical device QMS certificates have been issued worldwide

On Feb. 13, 2023, 33 nations sent their medical device regulators to Riyadh, Saudi Arabia, to participate in the Global Harmonization Working Party. The GHWP is a nonprofit organization that studies and recommends ways to harmonize global medical device regulations

The IAF was asked to participate and provide an update on the IAF CertSearch database, a global database where users can search and validate the status of accredited certificates issued by a certification body that has itself been accredited by an IAF-recognized accreditation body. The IAF presentation was provided by Nigel Johnston, who developed the database.

The presentation given to the GHWP members focused attention on the use of ISO 13485 and how the IAF CertSearch database is helping regulators to verify the credibility of these certificates. Johnston’s presentation raised alarms. He noted that the IAF CertSearch team had identified 20,000 fake or fraudulent certificates in the last year alone.

Although it isn’t fully populated (the database represents about 44% of all ISO QMS certificates included in the ISO Survey), it is now mandatory that accredited certification bodies upload them. Because of this requirement, this percentage is expected to increase significantly.

Source: https://www.qualitydigest.com/inside/fda-compliance-article/iaf-certsearch-team-identifies-20000-fake-or-fraudulent-iso-qms-certs