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Unprecedented times require innovative solutions to help meet business requirements. If you need Reg/Med Promo Review Support, let us know. OSR provides On-Demand Med/Reg Review Services.
Visit https://t.co/hSyPGTlReY to schedule a quick call and see how OSR can help.
#OSR
EXPERT MED/REG REVIEW SERVICES FROM ONESOURCE REGULATORY
We understand your challenge and are bringing expertise to the rescue.
OSR can provide flexible Med/Reg resources to assist your MLR process remotely.
Give us 15 minutes to explain how it works.
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Your Reg/Med Promo Reviewers are juggling many responsibilities during these unprecedented times. Interim support may be the thing you need. OSR provides On-Demand Med/Reg Review Services.
Visit https://t.co/ZX863i2JNp to schedule a quick call and see how OSR can help.
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Unprecedented times require innovative solutions to help meet business requirements. If you need Reg/Med Promo Review Support, let us know. OSR provides On-Demand Med/Reg Review Services.
Visit https://t.co/R3nSD4scDX to see how OSR can help!
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Your Reg/Med Promo Reviewers are juggling many responsibilities during these unprecedented times. Interim support may be the thing you need. OSR provides On-Demand Med/Reg Review Services.
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Take a look at a review of the ten enforcement letters sent by FDA's OPDP throughout 2019; including a breakdown of the violations cited. Similar to previous years, the primary focus in 2019 centered around the presentation of risk information.
https://t.co/z15CnQ6QfC
Through this study, OPDP hopes to better understand if the presence of a disclosure of payment status influences participant reactions. Currently, many celebrities publish posts with sponsored products and may or may not disclose as a paid advertisement.
https://t.co/HL3ERKplG8
Take a look at a summary of FDA's Office of Prescription Drug Promotion's (OPDP) 2019 enforcement activities. While still a relatively low amount, this year marks the third consecutive year seeing frequency of enforcement letters increase.
https://t.co/HL3ERKplG8
#FDA#OPDP
In an effort to determine how a drug name can affect how consumers and healthcare providers perceive the product, the FDA plans to launch a study asking 500 consumers and 500 healthcare providers to answer questions about seven different drug names.
https://t.co/HL3ERKplG8
https://t.co/HL3ERKplG8
FDA to Allow Online Submissions of Orphan Designation Requests
The shift on orphan drug designation request submissions follows the CDER's approval of more than twice as many orphan drugs in the past 8 yrs as in the previous 8.
#FDA#OrphanDrugs#OOPD
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This piece contains recent articles from leaders in the digital health space, focusing on what the changing digital health landscape, including big data, means for regulatory professionals.
https://t.co/WLuOpkBL0L
#DigitalHealth#BigData#SaMD#Cybersecurity
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