nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Advanced therapy medicinal products: Gene therapy
|
Ayala, Antonio |
|
2015 |
17 |
1-2 |
p. 253-264 |
artikel |
2 |
Chemical, pharmaceutical and biological information for medicinal products containing chemical and/or biological active substances
|
Übeda, Antonio Espinosa |
|
2015 |
17 |
1-2 |
p. 65-79 |
artikel |
3 |
Clinical trials
|
Pineda, Jaime Algorta |
|
2015 |
17 |
1-2 |
p. 117-152 |
artikel |
4 |
European pharmaceutical harmonisation
|
Sauer, Fernand |
|
2015 |
17 |
1-2 |
p. 9-15 |
artikel |
5 |
Herbal medicinal products
|
Gupta, Mahabir P. |
|
2015 |
17 |
1-2 |
p. 231-249 |
artikel |
6 |
Homeopathic medicines
|
Barelli, Bienvenido |
|
2015 |
17 |
1-2 |
p. 221-229 |
artikel |
7 |
Non-clinical reports
|
Herrera, Maria Dolores |
|
2015 |
17 |
1-2 |
p. 91-100 |
artikel |
8 |
Particular medicinal products
|
Ruiz-Bravo, Alfonso |
|
2015 |
17 |
1-2 |
p. 165-189 |
artikel |
9 |
Pharmaceutical products
|
Széliga, María Emilia |
|
2015 |
17 |
1-2 |
p. 81-89 |
artikel |
10 |
Prologue
|
Ramos-Cormenzana, Alberto |
|
2015 |
17 |
1-2 |
p. 5-7 |
artikel |
11 |
Registration dossier for radiopharmaceutical products
|
Mallol, J. |
|
2015 |
17 |
1-2 |
p. 213-220 |
artikel |
12 |
Regulatory harmonisation for better global health
|
Valverde, Jose Luis |
|
2015 |
17 |
1-2 |
p. 17-22 |
artikel |
13 |
Specific marketing authorisation dossiers and requirements
|
Asuero, A.G. |
|
2015 |
17 |
1-2 |
p. 155-161 |
artikel |
14 |
Specific requirements for somatic cell therapy medicinal products and tissue engineered products
|
Martín, Rosa M. Hernández |
|
2015 |
17 |
1-2 |
p. 271-277 |
artikel |
15 |
Specific requirements regarding module 4
|
González, Maria Dolores Herrera |
|
2015 |
17 |
1-2 |
p. 265-270 |
artikel |
16 |
Specific requirements regarding module 5
|
Hernández Martín, Rosa M. |
|
2015 |
17 |
1-2 |
p. 279-281 |
artikel |
17 |
Summary
|
Cabezas, María Dolores |
|
2015 |
17 |
1-2 |
p. 49-64 |
artikel |
18 |
The administrative information of the registration of a medicinal product dossier
|
Cabezas, María Dolores |
|
2015 |
17 |
1-2 |
p. 35-48 |
artikel |
19 |
The Common Technical Document as academic guideline
|
|
|
2015 |
17 |
1-2 |
p. 1-3 |
artikel |
20 |
The common technical document as basis of the authorization of marketing of medicinal products in the European Union
|
Cabezas, María Dolores |
|
2015 |
17 |
1-2 |
p. 23-31 |
artikel |
21 |
Toxicology
|
Zurita, Antonio Zarzuelo |
|
2015 |
17 |
1-2 |
p. 101-116 |
artikel |
22 |
1.2. Vaccines
|
Ruiz-Bravo, Alfonso |
|
2015 |
17 |
1-2 |
p. 191-212 |
artikel |