misswide

Travel, good food and Clinical Research. A few fantasy books throughn in for good measure. And yes, my tweets are my own.

[Premier Research @premierresearch]

Did you miss our recent webinar exploring gene therapies for Parkinson’s Disease?

Watch the full recording here: https://t.co/lPIw5hM83a

#ParkinsonsDisease #GeneTherapy

[Premier Research @premierresearch]

It's critical to incorporate patient safety and the patient perspective into the study design when developing a long-term follow-up strategy for a gene therapy trial. Read our experts' latest article in
@IntClinTrials. https://t.co/0RW1IXSOy1

[Premier Research @premierresearch]

Designing and conducting a #GeneTherapy trial is a complex undertaking. Read our latest blog exploring critical study design considerations of gene therapy trials and strategies for overcoming patient enrollment and safety challenges. https://t.co/bK2e3bjJHj

[Premier Research @premierresearch]

The global pandemic has exacerbated the challenges intrinsic to gene therapy trials. Read our blog highlighting strategies to ensure your trial’s operational efficiency and patient centricity. https://t.co/2FxHlgA6Bf #GeneTherapy

[Premier Research @premierresearch]

“Rare disease research provides hope to patients and families that are often overlooked. It gives them options and a way forward that would otherwise not have been there.” – Hanna Wide, Executive Director, Cell and Gene Therapy, Premier Research
#RareDiseaseDay

[misswide @HannaWide]

@AnnikaFLarsson And so many frustrations... 😂

[misswide @HannaWide]

@DouglassUla @shoegalhelsinki @ChrChristensen There hasn't been enough education in Sweden on how or why to where masks. Swedes do follow rules, but they have to make sense to them at the time.

[Premier Research @premierresearch]

For a condition that afflicts just one in 31,000 people, recruiting even 18 patients is a challenge. That's when we got creative. �� Case Study: From KOLs to Patient Advocates, Using Every Tool to Fight a Rare Disease https://t.co/KAXe9JtGQh

[Premier Research @premierresearch]

Looking for a CRO to conduct your next rare disease study? Come speak to the experts at Premier Research, booth #22, and find out how we can help put your next trial on the path towards success! #WODCEU

[misswide @HannaWide]

World Rare Disease Day 2018- who are you supporting today? #WRDD2018

[Rare Disease Day @rarediseaseday]

Have you signed up to the #RareDiseaseDay 2018 thunderclap campaign? On 28 February a message in support of the rare disease community will be shared on the social media accounts of everyone who joins! https://t.co/8USTc1oz0f #ShowYourRare @RareDiseases@raredisorders @RareVoices

[Rare Disease UK @rarediseaseuk]

We want to raise as much awareness as possible for #raredisease and #RareDiseaseDay! Please share our poster for 2018 to help us spread the word!

[Rare Disease UK @rarediseaseuk]

The average #raredisease patient waits 4 years before receiving a correct diagnosis. That's why we call it a 'diagnostic odyssey'.

[Premier Research @premierresearch]

Significant attention must be paid to the operational challenges within rare disease research. https://t.co/cb2wWjcReX