Search Result "Drug regulatory affairs"


Regulatory Affairs in Herbal Products

Ebook: Plant-derived Hepatoprotective Drugs

Volume: 1 Year: 2023
Author(s):
Doi: 10.2174/9789815079845123010007
Review Article

Regulatory and Quality Aspects of Herbal Drugs

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs (Discontinued)
Volume: 4 Issue: 2 Year: 2017 Page: 107-113
Author(s): Reena Hooda,Deepti Pandita,Poonam Kumari,Viney Lather

Review Article

Comparison of Regulatory Requirements for Registration of Pharmaceutical Drugs in Asean and GCC Regions

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs
Volume: 6 Issue: 1 Year: 2019 Page: 61-69
Author(s): Mohit,Aakash Deep,Gaurav Khurana,Jagdeep Kumar,Akshay Monga

Mini-Review Article

Regulatory Aspects of Personalised Medicines

Journal: Applied Drug Research, Clinical Trials and Regulatory Affairs
Volume: 8 Issue: 2 Year: 2021 Page: 77-83
Author(s): Ishita Dhingra,Neel Mani,Arti R. Thakkar

Review Article

Regulatory Approval of Silver Nanoparticles

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs
Volume: 5 Issue: 2 Year: 2018 Page: 74-79
Author(s): Richa Sood,Dimple S. Chopra

Review Article

Regulatory Requirements for Medical Devices: An Insight

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs (Discontinued)
Volume: 4 Issue: 1 Year: 2017 Page: 16-25
Author(s): Onkar Bedi,Pawan Krishan,Gaaminepreet Singh

Review Article

Comparative Study of Generic Drug Product Registration Requirements of Asean Countries with Specific Regulatory Process of Myanmar

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs
Volume: 5 Issue: 1 Year: 2018 Page: 4-12
Author(s): Janki Patel,Nilesh Prajapati,Mansi Paradkar

Research Article

Comparison of Regulatory Requirements for Filing Drug Master File (DMF) in Emerging Markets - China, Brazil & South Korea

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs
Volume: 7 Issue: 1 Year: 2020 Page: 71-81
Author(s): Kunta N. Reddy,Surenahalli G. Vasantharaju

Review Article

Regulatory Aspects of Post-Approval Safety Reporting for Generic Drug Products in the US

Journal: Applied Clinical Research, Clinical Trials and Regulatory Affairs (Discontinued)
Volume: 3 Issue: 3 Year: 2016 Page: 142-150
Author(s): Priti J. Mehta,Chandni K. Doshi

Review Article

In Silico Trial Approach for Biomedical Products: A Regulatory Perspective

Journal: Combinatorial Chemistry & High Throughput Screening
Volume: 25 Issue: 12 Year: 2022 Page: 1991-2000
Author(s): Della Grace Thomas Parambi

Previous   Next

Go To   Results 1 - 1 of 482

Filter Result

Volume Year
Content Type
Ads
© 2024 Bentham Science Publishers | Privacy Policy