Volume 7, Issue 3 , 2020
Genotoxic Impurities in Ranitidine Containing Products: An Overview
Pp: 155-161
Author(s): Shailesh Bhosale, Kamal Kant, Divya Goyal and Anoop Kumar*
DOI: 10.2174/2213476X07666200423081738
A Comprehensive Review of Regulatory Requirements and Registration Process of Pharmaceutical Drug Products in CIS Countries
Pp: 162-176
Author(s): Kapil Pihwal*, Neelam Pawar, Sheikh Aamir, Mohammad Shahbaz Alam and Vikas Rathee
DOI: 10.2174/2213476X07666200708105237
Safety and Quality of Nutraceuticals: Have FSSAI Guidelines been Able to Blaze the Trail?
Pp: 177-196
Author(s): Payal Dande*, Purva Samant, Yashita Singh and Umang Sheth
DOI: 10.2174/2213476X07666200825193259
Raw Data Management and Data Integrity in Pharmaceutical Product Development
Pp: 197-205
Author(s): Jenish Parmar, Priti Mehta*, Rajvi Patel, Manan Shah and Charmy Kothari
DOI: 10.2174/2213476X07999200901110354
Self-Emulsifying Drug Delivery System (SEDDS) and its Pharmaceutical Applications
Pp: 206-224
Author(s): Sankha Bhattacharya*
DOI: 10.2174/2213476X07666200827102951
Nanotechnology: Regulatory Outlook on Nanomaterials and Nanomedicines in United States, Europe and India
Pp: 225-236
Author(s): Rashi Malik* and Sharvil Patil*
DOI: 10.2174/2213476X06666191129094236
EU IVDR Regulatory Changes: An Overview of Requirements in (EU) 2017/746
Pp: 237-243
Author(s): Shashank Nayak*, M.P. Venkatesh and Pramod Kumar T.M
DOI: 10.2174/2213476X07666200327143023
Comparison of Maternal and Neonatal Outcomes in Case of Primary Cesarean Section Done During Late vs. Early Labor
Pp: 244-253
Author(s): Heena Anuff, Zeinah Rahman, Rajani Dube* and Shatha Taher Salman Al-Zuheiri
DOI: 10.2174/2213476X07666200708110738