015. Pharmacokinetics 2nd ed (1982).pdf
029. Controlled Drug Delivery - Fundamentals and Applications 2nd ed (1987).pdf
042. Topical Drug Delivery Formulations (1989).pdf
045. Biodegradable Polymers As Drug Delivery Systems (1990).pdf
049. Pharmaceutical Dissolution Testing (1991).pdf
050. Novel Drug Delivery Systems 2nd ed (1991).pdf
062. Drug Permeation Enhancement (1994).pdf
064. Achieving Sterility in Medical and Pharmaceutical Products (1994).pdf
065. Multiparticulate Oral Drug Delivery (1994).pdf
067. Pharmacokinetics Regulatory ú Industrial ú Academic Perspectives 2nd ed (1995).pdf
069. Good Laboratory Practice Regulations 2nd ed (1995).pdf
070. Physical Characterization Of Pharmaceutical Solids (1995).pdf
071. Pharmaceutical Powder Compaction Technology (1995).pdf
076. The Drug Development Process Increasing Efficiency and Cost Effectiveness (1996).pdf
081. Handbook of Pharmaceutical Granulation Technology (1997).pdf
083. Mechanisms of Transdermal Drug Delivery (1997).pdf
084. Pharmaceutical Enzymes (1997).pdf
085. Development of Biopharmaceutical Parenteral Dosage Forms (1997).pdf
087. Drug Products for Clinical Trials - An Intl Guide to Formulation, Production, Quality Control (1998).pdf
088. Development and Formulation of Veterinary Dosage Forms (1998).pdf
089. Receptor - Based Drug Design (1998).pdf
092. Pharmaceutical experimental design  (1999).pdf
095. Polymorphism in Pharmaceutical Solids (1999).pdf
097. Percutaneous Absorption Drugs-Cosmetics-Mechanisms-Methodology 3rd ed (1999).pdf
099. Protein Formulation and Delivery (2000).pdf
100. New Drug Approval Process 3rd ed (1999).pdf
102. Transport Processes in Pharmaceutical Systems (Marcel Dekker, 2000).pdf
103. Excipient Toxicity and Safety (1999).pdf
105. Pharmaceutical emulsions and suspensions (2000).pdf
106. Oral Drug Absorption - Prediction and Assessment (2000).pdf
107. Drug Stability - Principles and Practices 3rd ed (2000).pdf
108. Containment in the Pharmaceutical Industry (2001).pdf
109. Good Manufacturing Practices for Pharmaceuticals 5th ed (2000).pdf
110. Advanced Pharmaceutical Solids (2001).pdf
112. Pharmaceutical Process Engineering (2001).pdf
113. Pharmacogenomics (2001).pdf
114. Handbook of Drug Screening (2001).pdf
115. Drug Targeting Technology - Physical, Chemical and Biological Methods (2001).pdf
116. Drug - Drug Interactions (2001).pdf
117. Handbook of Pharmaceutical Analysis (2001).pdf
118. Pharmaceutical Process Scale-Up (2001).pdf
119. Dermatological and Transdermal Formulations (2002).pdf
120. Clinical Drug Trials and Tribulations 2nd ed (2002).pdf
121. Modern Pharmaceutics 4th ed (2002).pdf
122. Surfactants and Polymers in Drug Delivery (2002).pdf
123. Transdermal Drug Delivery 2nd ed (2003).pdf
124. Good Laboratory Practice Regulations 3rd ed (2003).pdf
125. Parenteral Quality Control - Sterility, Pyrogen, Particulate, and Package Integrity Testing (2002).pdf
126. Modified-Release Drug Delivery Technology (2003).pdf
127. Simulation for Designing Clinical Trials - A Pharmacokinetic-Pharmacodynamic Modeling Perspective (2003).pdf
128. Affinity Capillary Electrophoresis in Pharmaceutics and Biopharmaceutics (2003).pdf
129. Generic Drug Product Development - Solid Oral Dosage Forms 2nd ed (2013).pdf
129. Pharmaceutical Process Validation 3rd ed (2003).pdf
130. Ophthalmic Drug Delivery Systems 2nd ed (2003).pdf
131. Pharmaceutical Gene Delivery Systems (2003).pdf
132. Biomarkers in Clinical Drug Development (2003).pdf
133. Pharmaceutical Extrusion Technology (2003).pdf
134. Pharmaceutical Inhalation Aerosol Technology 2nd ed (2003).pdf
135. Pharmaceutical Statistics - Practical and Clinical Applications 4th ed (2003).pdf
136. Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics (2003).pdf
137. Freeze-Drying Lyophilization Of Pharmaceutical & Biological Products 2nd ed (2004).pdf
138. Supercritical Fluid Technology for Drug Product Development (2004).pdf
139. New Drug Approval Process, , Accelerating Global Registrations (2004).pdf
140. Microbial Contamination Control in Parenteral Manufacturing (2004).pdf
141. New Drug Development - Regulatory Paradigms for Clinical Pharmacology and Biopharmaceutics (2004).pdf
142. Microbial Contamination Control in the Pharmaceutical Industry (2004).pdf
143. Generic Drug Development- Solid Oral Dosage Forms (2004).pdf
145. Drug Delivery to the Oral Cavity - Molecules to Market (2005).pdf
146. Good Design Practices for GMP Pharmaceutical Facilities (2005).pdf
147. Drug Products for Clinical Trials 2nd ed (2006).pdf
148. Polymeric Drug Delivery Systems (2005).pdf
149. Injectable dispersed systems - formulation, processing, and performance  (2005).pdf
150. Laboratory Auditing for Quality and Regulatory Compliance (2005).pdf
151. Active Pharmaceutical Ingredients - Development, Manufacturing, and Regulation (2005).pdf
152. Preclinical Drug Development (2005).pdf
153. Pharmaceutical Stress Testing - Predicting Drug Degradation (2005).pdf
154. Handbook of Pharmaceutical Granulation Technology 2nd ed (2005).pdf
155. Percutaneous Absorption - Drugs, Cosmetics, Mechanisms, Methods 4th ed (2005).pdf
156. Pharmacogenomics 2nd ed (2005).pdf
157. Pharmaceutical Process Scale-Up 2nd ed (2005).pdf
158. Microencapsulation - Methods and Industrial Applications 2nd ed (2006).pdf
159. Nanoparticle Technology for Drug Delivery (2006).pdf
160. Spectroscopy of Pharmaceutical Solids (2006).pdf
161. Dose Optimization in Drug Development (2006).pdf
162. Herbal Supplements-Drug Interactions - Scientific and Regulatory Perspectives (2006).pdf
163. Pharmaceutical Photostability and Stabilization Technology (2006).pdf
164. Environmental Monitoring for Cleanrooms and Controlled Environments (2006).pdf
165. Pharmaceutical Product Development - In Vitro-In Vivo Correlation (2007).pdf
166. Nanoparticulate Drug Delivery Systems (2007).pdf
167. Endotoxins - Pyrogens, LAL Testing and Depyrogenation 3rd ed (2007).pdf
168. Good Laboratory Practice Regulations 4th ed (2007).pdf
169. Good Manufacturing Practices for Pharmaceuticals 6th ed (2006).pdf
170. Oral Lipid-Based Formulations - Enhancing the Bioavailability of Poorly Water-Soluble Drugs (2007).pdf
171. Handbook of bioequivalence testing (2007).pdf
172. Advanced Drug Formulation Design to Optimize Therapeutic Outcomes (2007).pdf
173. Clean-in-Place for the Biopharmaceutical Processes (2007).pdf
174. Filtration and Purification in the Biopharmaceutical Industry 2nd ed (2008).pdf
175. Protein Formulation and Delivery 2nd ed (2007).pdf
176. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms 3rd ed (2008).pdf
177. Dermal Absorption and Toxicity Assessment 2nd ed (2007).pdf
178. Preformulation solid dosage form development (2008).pdf
179. Drug-Drug Interactions 2nd ed (2007).pdf
180. Generic Drug Product Development - Bioequivalence Issues (2008).pdf
181. Pharmaceutical Pre-Approval Inspections - A Guide to Regulatory Success 2nd ed (2008).pdf
181. Preparing for FDA Pre-Approval Inspections - A Guide to Regulatory Success 2nd ed (2008).pdf
182. Pharmaceutical Project Management 2nd ed (2008).pdf
185. The Pharmaceutical Regulatory Process 2nd ed (2008).pdf
186. Handbook of Drug Metabolism 2nd ed (2008).pdf
187. Preclinical Drug Development 2nd ed (2009).pdf
188. Modern Pharmaceutics 5th ed Volume 1 - Basic Principles and Systems (2009).pdf
189. Modern Pharmaceutics 5th ed Volume 2 - Applications and Advances (2009).pdf
190. New Drug Approval Process (2009).pdf
191. Drug Delivery Nanoparticles Formulation and Characterization (2009).pdf
192. Polymorphism in Pharmaceutical Solids 2nd ed (2009).pdf
193. Oral Drug Absorption - Prediction and Assessment 2nd ed (2009).pdf
194. Biodrug Delivery Systems - Fundamentals, Applications and Clinical Development (2009).pdf
195. Pharmaceutical Process Engineering 2nd ed (2010).pdf
196. Handbook of Drug Screening 2nd ed (2009).pdf
197. Pharmaceutical Powder Compaction Technology (2011).pdf
198. Handbook of Pharmaceutical Granulation Technology 3rd ed (2009).pdf
199. Pharmaceutical Preformulation and Formulation 2nd ed (2009).pdf
200. International pharmaceutical product registration (2009).pdf
201. Generic Drug Product Development - International Regulatory Requirements for Bioequivalence (2010.pdf
202. Proteins and Peptides - Pharmacokinetic, Pharmacodynamic, and Metabolic Outcomes (2010).pdf
203. Pharmaceutical Statistics - Practical and Clinical Applications 5th ed (2009).pdf
204. Generic Drug Product Development - Specialty Dosage Forms (2010).pdf
205. Active pharmaceutical ingredients - development, manufacturing, and regulation (2010).pdf
206. Freeze-Drying Lyophilization Of Pharmaceutical & Biological Products 3rd ed (2010).pdf
207. Advanced Aseptic Processing Technology (2010).pdf
208. Sterile drug products - formulation, packaging, manufacturing, and quality (2010).pdf
210. Pharmaceutical Stress Testing - Predicting Drug Degradation 2nd ed (2011).pdf
211. Drug Stereochemistry - Analytical Methods and Pharmacology 3rd ed (2012).pdf
213. Handbook of Bioequivalence Testing 2nd ed (2015).pdf
214. Good Design Practices for GMP Pharmaceutical Facilities 2nd ed (2017).pdf
lista.doc