NOVEL CONSULTANTS

About Us

"Novel Consultants" is a team of expert Pharmaceutical Consultants headed by Mr. Nagesh Nanda.

1) Mr. Nagesh Nanda

Mr. Nagesh Nanda is a Freelance Consultant / Advisor to Pharmaceutical Industry and Academia worldwide with extensive contribution in drug product development, IVIVC evaluation and R&D Management concept.

Mr. Nagesh Nanda is a Post Graduate in Pharmaceutical Sciences (M.Pharma) as well as Masters in Business Administration (MBA) in Operations Management.

EXPERIENCE:

Mr. Nagesh Nanda has decades of work experience in India and Europe at senior management positions in Pharma MNCs.

ACHIEVEMENTS

• First Indian to be nominated for International Innovation Award in “Formulation Category” at CPhI Worldwide 2017, Frankfurt Germany.
• “Blue Resident Card Holder” of European Union, which is given to Intellectuals.
• Felicitated by Union Health Minister in June 2003 for outstanding contribution in the field of Pharmaceuticals.
• BIS Committee : Member of Bureau of Industrial Standards Committee for setting Quality Parameters for Choline Chloride (Vitamin B4) from 2001 to 2003.
• QCI : Member of Quality Council of India since inception till 2006.
• Former member of Indian Pharmacopoeia Committee.
• Suggested monographs to US Pharmacopoeia & British Pharmacopoeia for inclusion.

PROFESSIONAL EXPERTIZE (Partially Listed)

• Expert in establishing R&D Management system.
• Specialized in design and evaluation of Immediate & Modified Release pharmaceuticals, dissolution testing and technology, In-vitro In-vivo Correlation ( IVIVC), bioavailability/bioequivalence studies, Pharmacodynamic (Pd) clinical trials and regulatory considerations in pharmaceutical product development and evaluation.
• Assist/direct research teams in structuring and successfully analyzing intellectual property for innovativeness, non-infringement as well as validity analyses.
• Directed and executed over 400 bioavailability/bioequivalence studies & over 15 Pharmacodynamic studies for submission to regulatory agencies worldwide.
• Experienced in establishing infrastructure & system of R&D and Bio-evaluation Centers.
• Assist/direct in the preparation as well as facilitate for inspection by USFDA/EMA/MHRA/ANVISA/WHO/MCC/TGA etc. PAIs of manufacturing (API and finished dosage forms), laboratory and clinical sites.
• Ten patents for various research inventions are filed and six are already approved in various countries and rest are under evaluation.
• Invited speaker on national and international seminars and symposia.
• On board of three Universities in India for Pharmaceutical Science.
• External guide for PhD students in one of the University in India.