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M. P. Venkatesh

Publications (9)

A Comprehensive Outline of the Gulf Nations' Cosmetics Review and Approval Process: GSO Standards

G. Ramya Shree, M. P. Venkatesh & P. Subhash Chandra Bose · Asian Journal of Advanced Research and Reports · 2022

The GCC is an economic and political union of six countries: Bahrain, Kuwait, Oman, Qatar, Saudi Arabia, and the UAE. The council's main office is in Riyadh, Saudi Arabia. To ensure that cosmetic products are safe, the Gulf Cooperation Council Standardization Organization (GSO) r...

Open access Research Article 10.9734/ajarr/2022/v16i530471

China's Regulatory Change: The Evolution of National Medical Products Administration

M. Charmila, M. P. Venkatesh, N. Kavitha & Vedamurthy Joshi · Journal of Pharmaceutical Research International · 2022

The purpose of this paper is to provide an overview and review of the major regulatory changes that National Medical Products Administration has undergone in China since 2015 in order to accelerate new product production and registration in accordance with international standards...

Open access Research Article 10.9734/jpri/2022/v34i29B36051

Handling of Medical Devices: Reforms and Regulations

M. Charmila, M. P. Venkatesh & G. Ramya Shree · Journal of Pharmaceutical Research International · 2021

With the evolving technology and changing regulations, the medical device sector is set to grow quickly soon. Even though they are an integral part of patient care they present several unique problems which are not sufficiently addressed by the device manufacturer or the medical...

Open access Research Article 10.9734/jpri/2021/v33i60A34520

Comparison of Medical Device Regulations in India, Japan and South Korea

Chandan B. V., M. P. Venkatesh, Arjun M., Pasupuleti Dheeraj Krishna & Indraprasad S. · Journal of Pharmaceutical Research International · 2021

Increased health awareness, a growing middle class, and government health efforts are projected to propel India's medical equipment market forward in the next years. With the publication of the Medical Device Rules in 2017, Indian authorities revised the medical device regulatory...

Open access Research Article 10.9734/jpri/2021/v33i53A33634

Regulations for Testing and Licensing of Vaccines in United Kingdom

M. Ranjitha, H. R. Arjun & M. P. Venkatesh · Journal of Pharmaceutical Research International · 2022

Vaccines are one of the most significant achievements of science and public health for prevention of infectious disease. Overall vaccination policies for HCP in should be periodically revaluated in order to provide optimal protection against vaccine preventable diseases and infec...

Open access Research Article 10.9734/jpri/2022/v34i38B36224

Legislation and Regulation for Import Manufacture Distribution and Sale of Cosmetics in Sri Lanka

Akhilesh Akki, P. Subhash Chandra Bose, M. P. Venkatesh, K. Divith & Gorthi Nihar · Journal of Pharmaceutical Research International · 2021

The goal of cosmetics regulation is to provide Sri Lankans with safe and high-quality cosmetics that are equivalent to those in other nations. To accomplish these regulators and industry should collaborate to achieve common objectives. This category includes skin creams, lotions,...

Open access Research Article 10.9734/jpri/2021/v33i47B33095

Overview on Regulatory Requirements for Medical Devices in Srilanka - National Medicines Regulatory Authority/NMRA

Vishakharaju Motupalli, Subhash Chandra Bose, M. P. Venkatesh, Varsha Tiwari & Gembali Ramya · Journal of Pharmaceutical Research International · 2021

In the health-care industry, medical devices are becoming increasingly significant. One of the most challenging aspects of developing and manufacturing medical devices is keeping up with regulatory regulations and incorporating them into the process Registration, licensing, manuf...

Open access Research Article 10.9734/jpri/2021/v33i46B32978

Global Perspective of Paediatric Pharmacovigilance and its Importance: Where Have We Reached?

S. Narmada, M. P. Gowrav, Akhilesh Akki, Vishakharaju Motupalli, V. Balamuralidhara & M. P. Venkatesh · Journal of Pharmaceutical Research International · 2021

Pharmacovigilance is a tool proposed during the post-marketing process of the pharmaceutical product lifecycle to monitor drug safety in everyday life and to identify adverse drug reactions. The identification of adverse reactions, however, is a significant cause of concern and a...

Open access Research Article 10.9734/jpri/2021/v33i46A32867