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Journal of Pharmaceutical Sciences
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November 3, 2024
Experimental validation of a parenteral permitted daily exposure value for cleaning-induced degradants from recombinant therapeutic proteins with in vitro immunogenicity assays
Joseph R Cohen, Marisa K Joubert, Syeda Tabassum, et al.
Regulatory Toxicology and Pharmacology : RTP
|
June 12, 2020
Deriving harmonised permitted daily exposures (PDEs) for paracetamol (acetaminophen) CAS #: 103-90-2
Kamila Gromek, William Hawkins, Tanja Bernier, et al.
Journal of Pharmaceutical Sciences
|
September 18, 2022
Observation and Mitigation of Lamellar Silica Particles Formed in Pharmaceutical Products Packaged in Glass Vials
Yasser Nashed-Samuel, Jeremy Gastwirt, Ruchi B Kotia, et al.
Chemical Research in Toxicology
|
May 9, 2022
An Evaluation of the Occupational Health Hazards of Peptide Couplers
Jessica C Graham, Alejandra Trejo-Martin, Martyn L Chilton, et al.
Regulatory Toxicology and Pharmacology : RTP
|
June 2, 2024
Evaluation of the EMA log kow trigger for fish BCF testing based on data for several human pharmaceuticals
Lisa A Constantine, Natalie Burden, Todd Davidson, et al.
Environmental Toxicology and Chemistry
|
September 26, 2015
Use of acute and chronic ecotoxicity data in environmental risk assessment of pharmaceuticals
Jessica Vestel, Daniel J Caldwell, Lisa Constantine, et al.
Regulatory Toxicology and Pharmacology : RTP
|
August 14, 2022
Setting impurity limits for endogenous substances: Recommendations for a harmonized procedure and an example using fatty acids
Robert A Jolly, Suren Bandara, Joel Bercu, et al.
Environmental Toxicology and Chemistry
|
July 18, 2015
A risk-based approach to managing active pharmaceutical ingredients in manufacturing effluent
Daniel J Caldwell, Birgit Mertens, Kelly Kappler, et al.
Regulatory Toxicology and Pharmacology : RTP
|
October 10, 2020
Considerations when deriving compound-specific limits for extractables and leachables from pharmaceutical products: Four case studies
Patricia Parris, Elizabeth A Martin, Brad Stanard, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Journal of Pharmaceutical Sciences
|
November 3, 2024
Experimental validation of a parenteral permitted daily exposure value for cleaning-induced degradants from recombinant therapeutic proteins with in vitro immunogenicity assays
Joseph R Cohen, Marisa K Joubert, Syeda Tabassum, et al.
Regulatory Toxicology and Pharmacology : RTP
|
June 12, 2020
Deriving harmonised permitted daily exposures (PDEs) for paracetamol (acetaminophen) CAS #: 103-90-2
Kamila Gromek, William Hawkins, Tanja Bernier, et al.
Journal of Pharmaceutical Sciences
|
September 18, 2022
Observation and Mitigation of Lamellar Silica Particles Formed in Pharmaceutical Products Packaged in Glass Vials
Yasser Nashed-Samuel, Jeremy Gastwirt, Ruchi B Kotia, et al.
Chemical Research in Toxicology
|
May 9, 2022
An Evaluation of the Occupational Health Hazards of Peptide Couplers
Jessica C Graham, Alejandra Trejo-Martin, Martyn L Chilton, et al.
Regulatory Toxicology and Pharmacology : RTP
|
June 2, 2024
Evaluation of the EMA log kow trigger for fish BCF testing based on data for several human pharmaceuticals
Lisa A Constantine, Natalie Burden, Todd Davidson, et al.
Environmental Toxicology and Chemistry
|
September 26, 2015
Use of acute and chronic ecotoxicity data in environmental risk assessment of pharmaceuticals
Jessica Vestel, Daniel J Caldwell, Lisa Constantine, et al.
Regulatory Toxicology and Pharmacology : RTP
|
August 14, 2022
Setting impurity limits for endogenous substances: Recommendations for a harmonized procedure and an example using fatty acids
Robert A Jolly, Suren Bandara, Joel Bercu, et al.
Environmental Toxicology and Chemistry
|
July 18, 2015
A risk-based approach to managing active pharmaceutical ingredients in manufacturing effluent
Daniel J Caldwell, Birgit Mertens, Kelly Kappler, et al.
Regulatory Toxicology and Pharmacology : RTP
|
October 10, 2020
Considerations when deriving compound-specific limits for extractables and leachables from pharmaceutical products: Four case studies
Patricia Parris, Elizabeth A Martin, Brad Stanard, et al.
Page
of 2