Jyotsna Soneji (Borivali B 21 batch, 2019)

I had just completed M. Pharm and was considering Regulatory Affairs as a career option. IPM provided us with highly experienced faculty that gave us an insight into the real work with practical examples. The syllabus covered everything right from introduction upto final submissions. My concepts were clear which helped me for the interviews as well. Lastly, the team of Anagha Ma’am, Vidyesh Sir, Sheetal Ma’am is highly inspiring, who were always there to guide us.

Kanchan Parwani (Dombivli B 26 batch, 2019)

Myself Ms Kanchan Parwani have completed my Post Graduation as Masters of Pharmacy in Pharmaceutical Chemistry in 2010.

Some of the highlights starting in view of my career prospectus:

  • I joined a Pharmaceutical organization in 2010 in ADL, completing 5 years of experience in ADL, I worked as a Quality reviewer.
  • Next stage arrived to work as Deficiency response holder wherein I was involved to respond deficiencies from almost all agencies for final submission of the product. And there arrived an urge to join RA
  • After 8 years of experience, I joined IPM for PG Diploma in RA (Formulation and API).
  • Course has supported me to understand all the concepts of guidelines and importance of Regulatory towards any organization.
  • Finally, to a great success now joined as an RA professional in one of Pharmaceutical organization wherein I’m handling Post approval changes, Submissions, variations


Shobha Chaurasiya (Borivali B 20 batch, 2018)

I have total 10 years of experience in ADL department.

After completion of RA course from IPM, I got an opportunity to work in RA-API department.

I am thankful to IPM for their support and guidance.

Pranali Pingale (Dombivli B 25 batch, 2018)

I am Pranali Pingale from Thane. I have done my Post-graduation diploma in Regulatory Affairs from IPM Dombivli branch. I am very much thankful to IPM for giving me such wonderful knowledge regarding Regulatory requirements through this course. This knowledge is extremely helpful not only to regulatory affairs but also for all the departments involved in pharmaceutical industry.

The knowledge gained through IPM helped me a lot in my career as I got placed in Lupin through IPM.

As we see Regulatory is a very vast subject and critical to understand but the faculty arranged by IPM and Anagha ma’m herself made it very easy to understand.

Lectures arranged by IPM are in such a way that, it genuinely creates interest in Regulatory affairs.

I would like to suggest everyone to join IPM, who wants to grow their understanding and knowledge about pharmaceutical industry.

Again I am thankful to Anagha ma’m, Vidyesh sir, Sheetal ma’m and entire faculty of IPM for providing such a good base that would be very useful for us to grow.

Sayali Ranadive (Dombivli B 25 batch, 2018)

Hi friends… Welcome to IPM family!! I would like to take this opportunity to thank IPM team for such a wonderful experience of regulatory affairs (API and Formulation). we got over here. We started our journey with basics of ICH guideline which I feel is the pillar of RA. IPM professors are efficient, motivating and organized. They always used to tell us … if you want to get into this field all basic things should flow through your blood. IPM provides placement assistance to students to help them grow in their career.
Great is the art of beginning but greater is the art of ending. Three cheers to IPM!

Archana Pathak (Borivali B 18 batch, 2017)

I am thankful to IPM for organising courses like Post Graduate Diplomas. It is helpful for our career. My learning experience in IPM was excellent. The notes provided by them are easy to understand. The faculties involved have been truly helpful by sharing their knowledge and experience of industry with us. The knowledge gained through this education is always helping me in my day to day professional activities.
I wish a lot of thanks & best of luck to IPM for their future assignments. I would like to thank the entire IPM faculty starting from Anagha madam, Vidyesh sir and Sheetal for all the efforts.

Vishal Bankar (2017)
Manager, Cipla Dombivli B22 batch]
Course: PG Diploma in Regulatory Affairs

There are different training programs conducted by different individuals, industry experts or companies for RA with huge amount of fee on short topics or for single topic. But IPM offers all the regulatory topics with very small amount of fee, which if compared to given output negligible. The faculties are coming from different areas are armed with every part of guidance, ongoing practices and current agencies requirement.
I would recommend the IPM program to all RA professionals to get the expertise in all areas of regulatory, and to other segment from the pharma industry who wish to learn, who wish to join RA or who wants to upgrade our self in regulations.
In short, it is perfect blend of every ingredient (i. e. faculty, course structure, timing, notes, exam structure, discussion forum) needed for todays as well as future pharma industry; provided that each student should give his 100% efforts with consistency, dedication and full attention. As the course is important for freshers or professionals working in areas other than RA, it is equally important for those who are already working in RA.
Personally, I have five years of experience in Quality Assurance, but each time in every session, I learnt new aspects of guidance, new concepts which helped me to sharpen my present knowledge and to work on grey areas.
“Thank You IPM, Anagha, Vidyesh, Sheetal & team”.
Each RA professional must join & complete the course once in career.
All the best to students and IPM.


Emily Varghese (Distance Learning, 2016)
M. Pharmacy, student of distance learning program.

The course was very useful and helped me understand more about regulatory affairs. The notes were very helpful and it covered all the important topics related to regulatory affairs. I would strongly recommend this course to my friends.


Arpita Lahiri (Borivali B 16 batch, 2016)

I would like to start by thanking IPM for the quality learning and overall knowledge delivered.

I had about eleven years of experience in analytical research and development with no exposure in regulatory affairs directly. As I have worked extensively in ANDA projects, I felt RA would be a relevant field for me. But I was sceptic, can I really learn even one hundredth of the vast domain in just six months!! The subject is really vast but because of the syllabus designed by IPM, the lectures delivered by the faculties and the study materials provided, I am sure I have learnt a bit of it.

Not only the knowledge, the inspiration students get from IPM is quite amazing. I would specially thank the faculties for their extra ordinary lectures. Myself having vast experience in API never thought I would ever get a chance to work in formulation. I have got two offers in Regulatory affairs for quite senior roles in formulation.

I would say it is difficult to explore a new domain but it’s not impossible. I therefore would like to express my gratitude to IPM for everything that the institute and the people associate with the institute did for me.


Mansi Deshpande (Dombivli B 22 batch, 2017)

I am Mansi Deshpande from Dombivli. I am extremely overwhelmed to share with you that I got placed into Piramal as corporate regulatory affairs trainee and joined the office from 10th July, 2017.

I was able to present myself for this department just because of the knowledge and experience which IPM shared with me regarding regulatory field. I am really thankful to IPM team

I am grateful especially to Anagha ma’am, Vidyesh sir & Sheetal ma’am.

Thank you so much.


Prasad Bhat (Distance Learning, 2017)

I am Prasad Bhat, M.Pharmacy, student of distance learning program.

Course material isthorough and arranged in sequence provided. It covers all important topics of RA. Case studies and presentations are very effective. I received all updated guidelines via email so it’s very good practice to be updated with current scenarios.

Webinars are new to me. It’s a valuable experience.

IPM notifies available vacancies on regular basis. It is helpful for job seekers. It narrows the search for a good job opportunity.

All concepts of RA are crystal clear. Effective program even for distance learning.

It’s a wonderful experience to be a part of IPM and I will definitely recommend others to join IPM.


Debojyoti Adak (Distance Learning, 2013)
Regulatory Affairs Officer, LIFEPharma fze, Dubai
Course: PG Diploma in Drug Regulatory Affairs [Distance Learning]

I am really thankful to IPM for organising courses like Post Graduate Diplomas. It is really helpful for our career. Also thanks to IPM team as they have gathered and supplied the study materials in an organized way that helps us in our day-to-day job. These materials made easy to learn the topics. I wish that IPM can serve the pharma field like this for never ending way.

Debojyoti Adak


Jyoti Shelar, (Borivali B 10 batch, 2014)
Group Leader (QA), Enem Nostrum Remedies Pvt. Ltd
Course: PG Diploma in Drug Regulatory Affairs

IPM has been of great advantage to me where I have gathered knowledge of the overall view of a Pharma Industry. It has been of great assistance to me by including the keen topics related to Pharma (covering all guidance’s and procedures including almost every Regulatory aspect, ICH guidelines, etc).The faculties involved have been truly helpful by sharing their knowledge and experience of Industry with us. The experience and queries that were shared by Anagha madam were very interesting and developed interest to me for Regulatory affairs. Sincere thanks to every person involved in, from Anagha madam, Vidyesh sir, the entire faculty and Sheetal madam, for providing us with such a good base that will be fruitful to us in our near future.

Meena Mane (Borivali batch)
Course: PG Diploma in Drug Regulatory Affairs

My learning experience in IPM was excellent. Most of the professionals were subject matter expertise. IPM along with knowledge of regulatory affairs, imparts knowledge related to quality control, clinical, intellectual property, quality assurance and manufacturing in API as well as formulation. This helps the candidate to expand their vision in all different branches of Pharmaceutical industry. Also, there are regular updates on regulatory front in pharmaceutical industry to candidate. Thus, they take every initiative to keep their candidate acquainted with upcoming news in regulatory field regarding guidelines.
The notes provided by them are easy to understand and grasp. If any new topic apart from notes is presented in during lectures and candidate is interested in it, they make sure to forward to them.
It is my great pleasure to say something about Ms. Anagha Maharao using this platform. She is thorough with her technical and administrative expertise in regulatory field. Also, one of her specialty is that she never leaves room for the doubts. Which we find in her classroom sessions where she make candidate completely comfortable with subject by taking revision of previous lecture in next lecture before going ahead with any new topic.


Natasha Vadsariya

Natasha Vadsariya, B.Pharm (Borivali B 11 batch, 2014)
RA officer, Glenmark Generics Ltd.
Course: PG Diploma in Drug Regulatory Affairs

In this cut throat competition world, everyone is trying to leave their legacy and want to become something. That’s what even I’m trying to do. And I guess my journey has already begun when I came to know on 25th April, 2014 that I’m selected as regulatory affairs trainee in Glenmark generics. As a fresher, it’s difficult to get a regulatory job. Chances are very narrow.
But, sometimes you do make your way! It’s going to be a good head start to my regulatory affairs profession journey by joining as a trainee for 6 months in this reputed MNC. I wouldn’t have got this opportunity without the active placement facility of IPM. It’s all your hard work that makes you crack the interview but with proper direction and guidance from a mentor like Mrs Anagha Maharao, this process becomes a little easier!
Becoming a part of IPM family has given me lots of advantages like addition to my knowledge about drug regulatory affairs, interaction with finest people from industry, well arranged notes, flexible lecture timings, and opportunity to be the coordinator of the class and handle responsibility, doubt solving with personal attention of Anagha ma’m and lots more. I’ve got a good knowledge until now about ICH guidelines, CTD modules, US ANDA submissions and ongoing EUROPE submissions. I am sure remaining 2 months of my course will help me gain insight to remaining areas of drug regulatory affairs.
The distinguishing aspect of IPM is that they understand students need and they are willing to get better each day. For fresher 2013 pass outs like me, understanding regulatory affairs wasn’t so difficult. I assumed that regulatory affairs is going to be difficult for me seeing the notes when it was distributed for the first time, but with effective lectures by cooperative faculties helped me clear the concepts.

I want to thank Anagha ma’am, Sheetal ma’am, Vidyesh sir and the entire team of IPM for the efforts they are taking for the quality up gradation of the students.

Netra Dolhare, (Dombivli B 18 batch, 2015)
B.Pharm, Jondhale college of Pharmacy
Course: PG Diploma in Drug Regulatory Affairs

I would like to take this opportunity to thank Ms. Anagha Maharao and IPM team for doing a great job .It’s my pleasure that I am a part of IPM family. As a B.Pharm fresher, I was not acquainted with the industry as far the practical aspects of ADL & QC are concerned. The course has been designed very well for individuals who want to make a career in RA but also for individuals working in the various other departments (ADL,R&D,QC,QA) of the Pharma Industry and also for freshers.

While gaining the regulatory knowledge during the course, I am getting aware about the basic industry requirements and exact idea of work which I am going to do as RA professional in future. I am also very much thankful to Anagha mam, Vidyesh sir and Sheetal mam for giving me the biggest opportunity to help them as class coordinator as this is going to be an amazing experience from technical as well as from administrative point of view. I wish them all the very best for great success ahead for being a top most education institute worldwide!!



Priya D’souza (Dombivli B 17 batch, 2014)
Corporate QA, Cipla
Course: PG Diploma in Drug Regulatory Affairs

Regulatory Affairs being the backbone of every pharma industry, it is very important to understand the current regulations and guidelines and IPM helped me achieve this knowledge through the 6 months Drug RA course.
I sincerely appreciate Anagha ma’am and all the expertise from various pharma industries for the time spent in educating us and recommending strategies for achieving them.
This course engaged me in such a way that it provokes new ways of looking at things and challenges my own views.
The group discussion, brain storming sessions, team evaluation and self assessment made the class very interactive and interesting.
RA course has made a real difference in shaping my career and giving me a new perspective in life.
I would like to thank the entire IPM family starting from Anagha ma’am, Vidyesh sir and Sheetal ma’am for all the efforts put in bringing up this course.
I am now proud to say that I have successfully completed PG Diploma in Drug Regulatory Affairs through IPM and give an opportunity I would definitely like to take up another course through IPM again.

Ravindra More (Dombivli B 17 batch, 2014)
Corporate QA, Cipla
Course: PG Diploma in Drug Regulatory Affairs

RA course offered by IPM is very good blend of knowledge within short span of time. It is very difficult to cover all aspects within 6 months but IPM had made it very smooth and interactive sessions for which I was eager to attend every Sunday.
The knowledge gained from the course is showing fruits now, I am more confident now and growing immensely in my career.
I would like to thank the entire IPM faculty starting from Anagha madam, Vidyesh sir and Sheetal for all the efforts put in bringing up this course.



Shanu Baby, (Dombivli B 16 batch, 2014)
RA Associate, Glenmark Pharmaceuticals
Course: PG Diploma in Drug Regulatory Affairs

In this competitive world, getting a job is a highly privileged affair. Coming from a biotechnology background and with an experience in Business Development getting into mainstream pharma was always an uphill task and a dream. I was new to the pharma bubble and its regulations. That is when I came across IPM.

IPM was my stepping stone into the pharma industry and helped my career take off in the right direction. The syllabus structure is entirely job oriented which has tremendously helped me in my present work profile and day to day activities in the pharma field. The faculties are extremely knowledgeable and they are gems of knowledge which have been imparted onto me, which I will always cherish all through my years in the pharma industry.
I would like to thank Ms.Anagha, Mr.Vidyeshand Ms.Sheetal for initiating this venture and helping out all pharma aspirants by escalating their efficiency. I am extremely privileged to be a part of IPM family and would recommend this course to all.

Tanvee Deshpande, (Vashi B 08 batch, 2014)
F & D, Divakar Technospecialities and Chemicals,
Course: PG Diploma in Drug Regulatory Affairs

The most unique aspect of IPM is the Teaching Faculty. The didactic method of teaching including case studies, summarized notes and assessments are also the key factors of IPM! My regulatory affairs knowledge was enhanced mainly because of the highly experienced professors! IPM has given me a great platform to interact with my colleagues from various academic backgrounds and also with the teachers who have volunteered to teach at IPM. My experience with IPM will always be cherished since the environment has boosted my confidence has given me a lending hand to step in the Regulatory Market!



Kedar S.Raje, (Distance Learning, 2012)
Manager QA/QC,
Wanbury Ltd Mumbai

It gives me immense pleasure to announce Mrs. Anagha Maharao & her IPM team as one of the best institution to provide guidance & proper education in topic relevant to Pharmaceutical Industry. I have successfully completed PGD in Drug Regulatory Affairs & Diploma in Patent Laws under the kind guidance of Mrs. Anagha & her promising team. The knowledge gained through this education is always helping me in my day to day professional activities.
I wish a lot of thanks & best of luck to IPM for their future assignments. Let the flag of IPM fly higher & higher under the guidance of Mrs.Anagha.