Orphan drugs Social Media
Found 6 results for "Orphan drugs"Orphan drugs Hashtags 3 of 6
| Hashtag | Type | Description |
|---|---|---|
| #CoRDSchat | Healthcare Tweet Chats | orphan diseases, orphan drugs, Rare Disease, rare disease news, rare disease patient groups, rare disease research CoRDSchat is a live Twitter-driven event which takes place the last Friday of every month (Noon CST) CoRDSchat was founded by Liz Donohue, Director of… |
| #wcadvocacy | Healthcare Conferences | Patient Advocacy and Engagement 23rd September 2013 – 24th September 2013 advocacy, biotech, Medical Affairs, orphan drugs, pharmaceutical Advocacy • Engagement • Empowerment • Change Pharmaceutical and biotech companies are getting more in tune with patient engagement ev… |
| #2014GGSummit | Healthcare Conferences | Global Genes Patient Advocacy Summit 11th September 2014 – 13th September 2014 orphan drugs, Rare Disease Global Genes - Allies in Rare Disease: 2014 Rare Disease Patient Advocacy Summit will offer practical advice, case studies, and networking opportunit… |
| #CRDN15 | Healthcare Conferences | Cambridge Rare Disease Summit 2015 14th September 2015 genetics, investors, orphan drugs, patient advocacy, patient empowerment, pharmaceutical, Rare Disease, rare disease research Cambridge Rare Disease Network is holding its first annual conference, the Cambridge Rare Disease Summit 2015, at the Cambridge Judge Business School.… |
| #2015ggsummit | Healthcare Conferences | GlobalGenes 4th annual RARE Patient Advocacy Summit 24th September 2015 – 25th September 2015 FDA, orphan drugs, patient advocacy, pharma, Rare Disease The goal of this year’s RARE Patient Advocacy Summit is for patients, caregivers, and advocates to walk away equipped with actionable next steps whe… |
| #2016GGSummit | Healthcare Conferences | Global Genes Rare Patient Advocacy Summit 2016 22nd September 2016 – 23rd September 2016 orphan diseases, orphan drugs, patient advocacy, Rare Disease The 2016 Global Genes Rare Patient Advocacy Summit, September 22-23, offers practical next steps for rare disease organizations to take action in the … |
