We thank each and every participant
for making this event grand success.

// Janaury, 2015 //

Raaj GPRAC once again successfully conducted workshop of the series on “Summit for Global Regulatory Affairs strategies from Submissions, till Approvals and facing Challenges during Product Lifecycle Management" 9th, 10th & 11th January, 2015 at Hotel Satkar Residency,Thane Mumbai . The participants from Academic freshers and from Pharmaceutical companies like Adcock Ingram, Anthem biocell, GlaxoSmithKline, Brassica pharma, famycare, Sandoz ,Novartis India Ltd, Biotech Pharma & Nexus CRO etc. took advantage of the training. They enjoyed all the sessions along with the live examples & case study exercises. Raaj GPRAC thanks all the participants who have been a real driving force behind this training workshop.

// February , 2015 //

On 7th & 8th February 2015, Raaj GPRAC successfully conducted training for “Hands on CTD-eCTD submissions” at its Training Centre at Thane. Participants attended the training & gained fruitful practical experience of eCTD dossier preparations for US & EU.

// October, 2015 //

On 24th & 25th October 2015, Raaj GPRAC successfully conducted its next training for “Hands on CTD-eCTD submissions” at its Training Centre at Thane. Candidates of India enjoyed the training & practical experience of eCTD dossier preparations for US & EU.

// July, 2015 //

On 10th & 11th July 2015, Raaj GPRAC successfully conducted its next training for “Hands on CTD-eCTD submissions” at its Training Centre at Thane. Candidates of USA enjoyed the training & practical experience of eCTD dossier preparations for US & EU.

// December, 2015 //

Raaj GPRAC was proud to present its Workshop on ‘’FDA Regulations with GMP and Quality System’’ which was held at KOB Medical Textile Pvt. Ltd on 21st & 22nd Dec 2015. This workshop featured with keynote addresses, presentations, case studies, Quiz and interactive discussions from FDA history, Overview of Medical Devices, 510(k), PMA, Overview of GMP, Validations, CAPA, Types of Audits, Methodology, How to face Audits, How to answer 483’s, Quality Risk Management, Post inspections, approval, implementation and maintenance of GMP by audits. Almost 27 Empolyees have taken advantage of this important traning.