nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Application of the euglycaemic clamp technique to bioassay of insulin analogues
|
Vølund, A. |
|
1992 |
20 |
2 |
p. 135-142 8 p. |
artikel |
2 |
Detoxification of diphtheria and tetanus toxin with formaldehyde. detection of protein conjugates
|
Aggerbeck, Henrik |
|
1992 |
20 |
2 |
p. 109-115 7 p. |
artikel |
3 |
International workshop: ‘Poliovirus attenuation: Molecular mechanisms and practical aspects’
|
Ehrenfeld, Ellie |
|
1992 |
20 |
2 |
p. 167-169 3 p. |
artikel |
4 |
Note for guidance
|
Committee for Proprietary Medicinal Products: Ad Hoc Working Party on Biotechnology/Pharmacy and Working Party on Safety Medicines, |
|
1992 |
20 |
2 |
p. 159-164 6 p. |
artikel |
5 |
Note for guidance
|
Committee for Proprietary Medicinal Products: Ad Hoc Working Party on Biotechnology/Pharmacy and Working Party on Safety Medicines, |
|
1992 |
20 |
2 |
p. 155-158 4 p. |
artikel |
6 |
Obituary—Jean-Pierre Lecocq 1947–1992
|
Horaud, Florian |
|
1992 |
20 |
2 |
p. 89- 1 p. |
artikel |
7 |
Potency assays for anistreplase: Comparison of the fibrin plate assay and a 96-well plate assay
|
Beebe, Deborah P. |
|
1992 |
20 |
2 |
p. 129-133 5 p. |
artikel |
8 |
Quantitative estimation of diphtheria and tetanus toxoids. 6. Use of different antibody titration methods for evaluation of immunogenicity in animals during potency assay of diphtheria toxoid
|
Lyng, Jørn |
|
1992 |
20 |
2 |
p. 101-108 8 p. |
artikel |
9 |
Report of a collaborative study to assess the determination of glycoprotein antigen content of rabies vaccines for human use
|
Ferguson, Morag |
|
1992 |
20 |
2 |
p. 143-154 12 p. |
artikel |
10 |
Safety aspects in the manufacturing of plasma-derived coagulation factor concentrates
|
Burnouf, Thierry |
|
1992 |
20 |
2 |
p. 91-100 10 p. |
artikel |
11 |
Variation in the biological function of envelope protein epitopes of yellow fever vaccine viruses detected with monoclonal antibodies
|
Ledger, T.N. |
|
1992 |
20 |
2 |
p. 117-128 12 p. |
artikel |
12 |
Views on the issues raised in recent letters by Galibert recommending studies for genetic stability testing of cells used to manufacture purified polypeptide pharmaceutical products utilizing recombinant DNA (rDNA) technology
|
Committee on Process Development and Manufacturing, |
|
1992 |
20 |
2 |
p. 165-166 2 p. |
artikel |