Incoming Resources
- Optimization of Pharmaceutical Processes, edited by Antonios Fytopoulos, Rohit Ramachandran, Panos M. Pardalos
- Group Sequential and Confirmatory Adaptive Designs in Clinical Trials, by Gernot Wassmer, Werner Brannath
- Statistical Remedies for Medical Researchers, by Peter F. Thall
- A Practical Guide on Behaviour Change Support for Self-Managing Chronic Disease, edited by Mara Pereira Guerreiro, Isa Brito Félix, Marta Moreira Marques
- Ways of Regulating Drugs in the 19th and 20th Centuries, edited by Jean-Paul Gaudillière, Volker Hess
- Pharmacovigilance in the European Union, Practical Implementation across Member States, by Michael Kaeding, Julia Schmälter, Christoph Klika
- Pharmacy and Professionalization in the British Empire, 1780-1970, by Stuart Anderson
- Practical Considerations for Adaptive Trial Design and Implementation, edited by Weili He, José Pinheiro, Olga M. Kuznetsova
- Innovating in a Learning Community, Emergence of an Open Information Infrastructure in China's Pharmaceutical Distribution Industry, by Kai Reimers, Xunhua Guo, Mingzhi Li, Bin Xie, Tiantian Zhang
- Pharmacologia, or, the history of medicinal substances, John Ayrton Paris
- Quantitative Decisions in Drug Development, by Christy Chuang-Stein, Simon Kirby
- Handbook of Substance Misuse and Addictions, From Biology to Public Health, edited by Vinood B. Patel, Victor R. Preedy
- Healing Springs of Russia, by Svetlana Malkhazova, Dmitry Orlov, Natalia Shartova, Sergey Starikov, Tatiana Puzanova
- Statistical Applications for Chemistry, Manufacturing and Controls (CMC) in the Pharmaceutical Industry, by Richard K. Burdick, David J. LeBlond, Lori B. Pfahler, Jorge Quiroz, Leslie Sidor, Kimberly Vukovinsky, Lanju Zhang
- Market Access of Traditional Chinese Medicinal Product in the EU under WTO Legal Framework, by Saisai Wang