Drug Delivery and Nanomedicine

July 18-20, 2022 | USA

Drug Delivery
After a successful Drug Delivery Webinar 2021 during March and August 2021. it is our greatest pleasure to welcome you to the 5th Edition of Drug Delivery Webinar planned to be organized during  July 18-20, 2022.
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Spotlight

Development and production of biopharmaceuticals are complex. Even minor impurities, orchanges in attributes such as glycosylation or charge heterogeneity, can have a profound impact on the safety and = ef cacy of the nal product. Traditionally, multiple analytical techniques have been required to assess the full range of biopharmaceutical product attributes. But the inevitable consequence of multiple analytical techniques is greater expenditures of time and resources.


OTHER UPCOMING CONFERENCES

Drug Discovery And Communal Trial

August 27-28, 2022 | Malaysia

Association of Pharmaceutical Research (APR) organizes the “Pharma Summit 2022: Drug Discovery & Communal Trial” on 27th & 28th August 2022, in Kuala Lumpur, Malaysia.
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World Drug Safety Congress Europe

September 27-29, 2022 | USA

The World Drug Safety Congress Europe is empowering patients, physicians, pharma, biotech and consumers to make the best drug safety decisions.
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3rd European Congress on Pharmaceutical Science And Research

August 15-16, 2022 | Singapore

PHARMACEUTICAL SCIENCE 2022 welcomes attendees, presenters, and exhibitors from all over the world to Singapore. We are delighted to invite you all to attend and register for the “3rd European Congress on Pharmaceutical Science & Research” which is going to be held during August 15-16, 2022 in Singapore.
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16th World Drug Delivery Summit

October 28-29, 2022 | Canada

Conference Series LLC Ltd with great pride and honour announcing its "16th World Drug Delivery Summit " (Drug Delivery 2022), which is going to be held during October 28-29, 2022 Vancouver, Canada and invite all the participants all around the world. The theme of the conference is “Advancement in the Technologies used in Drug Delivery”.
Register Now

Spotlight

Development and production of biopharmaceuticals are complex. Even minor impurities, orchanges in attributes such as glycosylation or charge heterogeneity, can have a profound impact on the safety and = ef cacy of the nal product. Traditionally, multiple analytical techniques have been required to assess the full range of biopharmaceutical product attributes. But the inevitable consequence of multiple analytical techniques is greater expenditures of time and resources.

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