Relevant publications

Marr, A.P. (2012)Impact of the reduced requirements for the Eudravigilance medicinal product dictionary

Scrip Regulatory Affairs, Apr 2012, 15-17

2012
Marr, A.P. (2011)EMA sheds new light on requirements for the Eudravigilance medicinal product dictionary

Scrip Regulatory Affairs, Oct 2011, 11-14

2011
Marr, A.P. (2011)EMA mandates Eudravigilance medicinal product dictionary for all authorised products in Europe

Scrip Regulatory Affairs, Aug 2011, 14-17

2011
Marr, A.P. (2010)ICH progresses new standards for the Individual Case Safety Report and unambiguous identification of medicinal products

Pharmacovigilance Review, 4 (3), 7-9

2010
Marr, A.P. (2010)The European e-submission experience : An applicant’s view of different procedures.

Regulatory Focus, 15 (6), 8-13

2010
Marr, A.P.; Page, K.J. & Williams, G.K. (2010)A Future for NeeS

Regulatory Affairs Journal, 21 (4), 211

2010
Holmes, C; Marr, A.P.; Menges, K; Kaindl, T.; Franken, A.; Gould, M. & Gibbard, M (2010)PIM – the EU’s planned default process for product information submission and management.

Regulatory Rapporteur, 7 (1), 4-7

2010
Page, K.J.; Marr, A.P. & Williams, G.K. (2010)Is Europe ready for eCTD? An industry perspective.

Regulatory Rapporteur, 7 (1), 8- 11

2010
Buxton, T & Marr, A.P. (2005)PIM – a new method for the submission of product information in the Centralised Procedure

Regulatory Rapporteur, 2 (4), 12-15

2005
Marr, A.P. (2002)The specification for the electronic Common Technical Document (eCTD) – your chance to comment.

ESRA Rapporteur, 9 (4), 4-7

2002
Marr, A.P. (2002)Letter to the Editor

The Regulatory Review, 5 (7), 31

2002
Marr, A.P. (2001)The electronic Common Technical Document – Why is it needed and what is it likely to contain?

Regulatory Affairs Focus, 11 (3), 11-15

2001
Marr, A.P. (2001)The impact of ICH M2 and the eCTD: Current status and future directions

In : Fulfilling the potential of electronic interactions between the pharmaceutical industry and regulatory authorities : Issues and initiatives, Publ. CMR International, pp 7-13

2001