MedCity News
OCTOBER 2, 2022
The key reasons for patient satisfaction with telehealth was having adequate facetime, the report said. Those who were ranked high spent enough time providing quality care, explained health concepts clearly and completely resolved medical issues on the first visit.
PharmaTech
OCTOBER 2, 2022
FDA backs joint reviews, common research policies, and modern production methods around the world.
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
MedCity News
OCTOBER 2, 2022
Virginia-based Careviso recently raised $17 million in Series B funds. The company — which is focused on improving transparency and access for diagnostic testing — will use the funds to enhance its platform’s price transparency tool and deploy it in physician offices so it can be used at the point of care.
PharmaTech
OCTOBER 2, 2022
Codex DNA’s BioXp 9600 system is designed for the automated synthesis of synthetic biology workflows.
Advertisement
Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud
MedCity News
OCTOBER 2, 2022
Sudo Bioscience emerged with $37 million in funding and four programs that address TYK2, a promising target for autoimmune diseases. Bristol Myers Squibb drug Sotyktu recently won the first FDA approval for a TYK2 inhibitor but Sudo claims its molecules have the potential to be best in this new drug class.
PharmaTech
OCTOBER 2, 2022
Under the revised NIS-2 Directive in Europe, pharma companies will need to be proactive in safeguarding their digital assets.
Pharma Rep Focus brings together the best content for pharma rep professionals from the widest variety of industry thought leaders.
PharmaTech
OCTOBER 2, 2022
Susan J. Schniepp, distinguished fellow at Regulatory Compliance Associates, addresses the difference between regulatory compliance and real compliance.
Pharmacy Times
OCTOBER 2, 2022
As individuals in a society, all people have implicit, or unconscious, beliefs that they have been socialized to hold; however, health care professionals’ implicit biases can impact patients’ lives.
PharmaTech
OCTOBER 2, 2022
L.B. Bohle’s QbCon 1 is intended to meet all quality requirements for long granulation processing time.
PharmaTech
OCTOBER 2, 2022
The new inorganic pyrophosphate from Canvax is intended for use in RNA IVT reactions.
Advertisement
Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.
PharmaTech
OCTOBER 2, 2022
The 1VQ papers advocate for the idea that certain post-approval changes should be streamlined and expedited.
PharmaTech
OCTOBER 2, 2022
ROSS Ribbon Blenders are a customizable solution designed to minimize risk and maximize productivity.
PharmaTech
OCTOBER 2, 2022
One can only learn the secrets of "fight club" by attending its meetings.
Expert insights. Personalized for you.
93 
Let's personalize your content