00007_CTD eCTD regulatory submissions

Raaj GPRAC presents hands on training in CTD/eCTD regulatory submission to USFDA and Europe.
We are RA and GMP consultants and TRAINER in Pharma, Biotech industry and BPO/KPO/CRO .
We offer all industrial and job-related training programmes and PG Diploma in Regulatory Affairs, Quality assurance, Clinical Research, PharmacoVigilance, Patents, Pharma Documentation, Pharma Management, GLOBAL Regulatory affairs, Medical Writing etc.
Please come and join us at www.rajgprac.com,
Contact us at [e-mail], [e-mail],
Call us on 022 65619030/ 25445541/ 9821144706.
Thanks,
Rajashri Ojha
Founder and Director,
Raaj GPRAC
Skype-rajashri.ojha
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[@rupeshbhawsar7268]

thanks mam.....!! very interesting session ..!!

[@thaggedele8476]

Thanks for Uploading this video ...Great lecture by madam....Please could you send me the PPT madam, I am Also from same Professional....

[@NeelGangradeofficial]

can we have more sessions ? :) great job !!

[@rajashriojha9139]

Please give me your email id and whats app number to send the online procedure. Visit our website at www.raajpharmaelearning.com