MEDICAL DEVICE REGULATIONS
Interactive Session with Regulators on Legal Metrology Rules for Medical Device Sector
Program Objective
The Department of Consumer Affairs has recently announced that all Medical Devices must contain information about the Retail Price, the Place of Origin, Size and Dimensions, and Consumer Care Information on the Product Package.
As per the announcement, it was required by the Legal Metrology (Packaged Commodities) Rules, 2011, that every packaged good, including Medical Devices, bear such information on them or on a Label firmly attached to the Device.
The provisions requires declaration of mandatory information including Retail Sales Price in the form of MRP, Country of Origin, Size and Dimensions of the Commodity where the sizes of the commodity in the package are relevant, Unit Sale Price and Consumer Care details, on the pre-packaged commodities based on which the Consumer can take an informed decision.
For various offenses, such as selling above MRP in Hospitals, Retail Locations, or on
e-commerce platforms, altering MRP or other declarations/without declarations, etc., enforcement provisions are made under the Legal Metrology Act/Packaged Commodities Rules in order to protect Consumer Rights.
The provisions of the Legal Metrology Act are also applicable on sale of products in loose or without packaging and sale through E-commerce websites in the interest of Consumers.
Hence a session is organised to create an awareness to industry members and stakeholders connected to Medical Device sector about Legal Metrology Rules as well as Compliance to Labeling requirement of similar nature from the Medical Device Rule 2017.
Download the Program Brochure
REGISTRATION DETAILS
Fee :
No Fee. Session open for all.
Who can Register ?
Individuals who use any weight or measure for a transaction or industrial production
Manufacturers , Importers & Retailers, Dealers, Distributors, resellers, stockiest, exhibitors etc. who work with weight, measure or number-related items in Medical Device Sector.
Hospitals and other Healthcare Service Organizations which deal with Medical Devices – Sell Medical Devices, act as Resellers, Importers, Distributors, handle Retail sales etc
Management Systems Consultants, Regulatory Affairs Professionals , EXIM Consultants, Legal Professionals
Certification Bodies, Inspection Bodies , Testing Labs
Academia – Research & Innovation Institutions in Medical Device space
Startups, Innovators in Medical Device Sector
All registered delegates will receive confirmation message directly from Zoom. Both AIMED and Consultants Consortium of Chennai will send confirmation mail to all delegates 1 day before the program date.
Contact Coordinate – CCC Secretariat :
Mrs Rama Venugopal
Email : contact@ccc-consultants.org ; communication@cccassociation.org
Whatsapp : +91 73389 92778 +91 9840870532
Share your queries in advance related to Legal Metrology Rules to :
Request Industry Members to share their questions (if any), related to Implementation of Legal Metrology and Packaging Rules to following co-ordinate at AIMED Secretariat :
AIMED Secretariat :
Mr. Chitta Ranjan Biswal,
Technical Officer
Email : forumcoordinator@aimedindia.com
is this registration applicable if selling the goods through Distributor and if selling the product on FOC (spares) directly to end customer
we will include your question for Q&A Session . Let the Regulators clarify it
We are basically Ventilator Manufacturing Company. its active medical device. is it necessary to display the price on label?.
because it will vary depending on Qty purchased / customer to customer. in this kind of scenario, what we should do?
we will include your question for Q&A Session . Let the Regulators clarify it