This document outlines the process for obtaining registration and a license for medical devices and diagnostics in India. It describes the key regulatory body, the application process through the Sugam online portal, required documents which include product details, regulatory status and certificates, and fees. It then explains the review process, including potential resubmission if queries are raised, and specifies that the licensing authority aims to grant the license within 9 months of the application submission.
This presentation is in continuation of my previous ppt on the same topic.
Now CCIM changed the process and make it online only process.
Important Notice- The fee required for central registration may change any time, please check it before going online
Cashless treatment facilities for emergency and chronic disease are now available for U.P. government employees and pensioners.
This simple procedure can be adopted by anyone.
This presentation is in continuation of my previous ppt on the same topic.
Now CCIM changed the process and make it online only process.
Important Notice- The fee required for central registration may change any time, please check it before going online
Cashless treatment facilities for emergency and chronic disease are now available for U.P. government employees and pensioners.
This simple procedure can be adopted by anyone.
It is very important having software like leave management.In such kind of software can easily maintain leaves of your employes.Leave Management Software is easy to install and user friendly software and can be customized on windows applications.
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For better user management, tracking and KYC compliance, the changes that have recently been done in Naukri Recruiter system:-
1. New Interface for Manage Users
2. User creation and mandatory verification
3. User deletion and Resdex Rights revocation
4. Password related changes
It is very important having software like leave management.In such kind of software can easily maintain leaves of your employes.Leave Management Software is easy to install and user friendly software and can be customized on windows applications.
Resdex Enhanced Security using Login OTP for sub usersvridhi chowdhry
Additional layer of security using One-Time Password (OTP) for login whenever login pattern of users change.
This will help prevent unauthorized access in Naukri.com sub user accounts.
For better user management, tracking and KYC compliance, the changes that have recently been done in Naukri Recruiter system:-
1. New Interface for Manage Users
2. User creation and mandatory verification
3. User deletion and Resdex Rights revocation
4. Password related changes
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The norm in Nigeria with regards to recruitment of unemployed persons is that majority of recruitment agencies make promises of employment to unsuspecting job seekers which in most cases are non-existent and demand high consulting fee for such unscrupulous service. It is then crucial for companies or organizations keen on operating recruitment service as a recruitment agency or to function as a recruiter in any capacity in Nigeria to comply with the provisions of the Labour Act, CAP L1, LFN 2004, and obtain a RECRUITERS LICENSE from the Ministry of Labour and Employment.
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
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June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
unwillingness to rectify this violation through action requires accountability.
Postsecondary education is a unique opportunity for students to learn and have their ideas and beliefs challenged. However, universities receiving hundreds of millions of federal funds annually have denied
students that opportunity and have been hijacked to become venues for the promotion of terrorism, antisemitic harassment and intimidation, unlawful encampments, and in some cases, assaults and riots.
The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
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Biological screening of herbal drugs: Introduction and Need for
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The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
For more information, visit-www.vavaclasses.com
2. INTRODUCTION
• In India, the manufacturing, import, sale, and distribution of medical devices
are regulated under India’s Drugs & CosmeticAct and Rules (DCA).
• The Central Drug Standards Control Organization (CDSCO) isIndia’s
main regulatory body for pharmaceuticals and medical devices.
• Any person who intends to manufacture a Class A or Class B medical device
including in vitro diagnostic medical deviceshall make an application for
grant of license to the State Licensing Authority.
3. PROCESS FOR MEDICAL DEVICE &
DIAGNOSTIC REGISTRATION
1. Create Login Id by filling the Registration form on Sugam Portal.
2. Username will be corporate email id and it should be unique, which can be used
as user name for future communication.
3. Password length should be at least six characters with at least one number,one
lowercase, one uppercase letter and one special character.
4. Upload necessary documents.
5. After clicking on "Submit" button, a confirmation link will be sent to user’s
registered email id to verify registration.
6. Verify account by clicking on the link sent to the registered email id.
7. After clicking the verification link, registration application of the user will be sent
for approval to the concerned authority.
8. In case of approval/rejection of the application, a mail will be sent to user's
4. registered email id.
9. After receiving approval mail from CDSCO for their user registration, User can
login into the system with User Name and Password as entered in user
registration
5. APPLICATION
After completion of login procedure, application shall be file in Form 40 for Fresh
Registration.
DOCUMENTS REQUIRED
1. Covering Letter-Purpose should be clearly mentioned with page numberand
Index.
2. Self-attested copy of authorization letter to the person issued by the
Director/Company Secretary/Partner of the Indian Agent firm.
3. Detail Product description along with material of construction, intendeduse,
Product specification, product literature, package inserts alongwith a sample.
4. Regulatory status of the said product in country of origin.
5. Regulatory certificates in respect of said product.
6. FEES: 1000 USD for each product.
The licensing authority shall within 9 months from the date of receipt ofapplication
issue such Registration Certificate, which may extend further for not more than
3months.
7. SUBMISSION
FINAL PREVIEW
Once payment is done user can view the complete legal form with payment details
and download the system generated form for signature.
SUBMISSION OF FORM
1. Take print of downloaded system generated form.
2. Sign & Scan form.
3. Upload the document after which the form will be submitted.
After submission of form a file number will generate which will be used fortracking
of application.
8. REVIEW
APPLICATION RECEIVED BY NODAL OFFICER
After successful submission of application, the application will be received by Nodal
Officer, who shall forward the same to Reviewing Officer.
APPLICATION REVIEW
After receiving the application from Nodal Officer, Reviewing officer will check the
application & if it is completed in all respect, he shall forward the application to
Deputy Decision Authority with his comments upon it.
9. RESUBMISSION
1. The Deputy Decision Authority will raise query, if any & sent intimation
to applicant.
2. If Documents are in Order, then forward the application toLicensing
Authority.
10. GRANT OF LICENSE
After receiving the application from The Deputy Decision Authority , the
Licensing Authority will Grant License.
Within 9 months from the submission of application License will be granted.
*The licensing authority shall within 9 months from the date of receipt of
Application issue such Registration Certificate, which may extend further for not
more than 3 months.
* License will remaining valid for the period of 3 years.
*Applications for Renewal of License should be submitted minimum 9 months
Before the expiry of the registration certificate.