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David G Dolan

Showing results (11-20 of 19) with videos related to

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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 assaysJoseph 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 #: 103-90-2Kamila 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 VialsYasser 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 CouplersJessica 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 pharmaceuticalsLisa 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 pharmaceuticalsJessica 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 acidsRobert 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 effluentDaniel 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 studiesPatricia Parris, Elizabeth A Martin, Brad Stanard, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 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 assaysJoseph 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 #: 103-90-2Kamila 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 VialsYasser 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 CouplersJessica 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 pharmaceuticalsLisa 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 pharmaceuticalsJessica 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 acidsRobert 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 effluentDaniel 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 studiesPatricia Parris, Elizabeth A Martin, Brad Stanard, et al.
Pageof 2