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pCPA announces new three-year pricing initiative agreement for generic drugs with CGPA, appointment of Douglas Clark as its first CEO | Smart & Biggar

The pan-Canadian Pharmaceutical Alliance (pCPA) and the Canadian Generic Pharmaceutical Association (CGPA) have agreed to a new three-year pricing initiative for generic drugs,. ....

Douglas Clark , Ontario Exceptional Access Program , Canadian Pharmaceutical Alliance , Canadian Generic Pharmaceutical Association , Tiered Pricing Framework , Canadian Select Molecules , Patented Medicine Prices Review Board ,

As a Thunder Bay man battles a rare cancer, his family fights to get $300K treatment covered

The family of a 30-year-old man in Thunder Bay, Ont., who's fighting a rare form of cancer is waging a battle of their own: Trying to get funding for his treatments, which cost $9,000 each. ....

Thunder Bay , Patty Hajdu , Lauri Mcfarlane , Durhane Wong Rieger , Jonathan Mcfarlane , Lise Vaugeois , Organization For Rare Disorders , Ontario Exceptional Access Program , Ministry Of Health , National Strategy For Drugs , Thunder Bay Regional Health Sciences Centre , Canadian Organization For Rare Disorders , Canadian Cancer Society , Canadian Association For Rare Disorders , Health Canada , Ontario Health , Go Fund Me Kristen Chlebovec , Canadian Association , Cancer Care , Kristen Chlebovec , Joseph Del Paggio , Del Paggio , Rare Disorders , National Strategy , Canadian Organization , Exceptional Access Program ,

Woman with cystic fibrosis previously denied gets game-changing drug

Sara Aldrich s application for provincial coverage for Trikafta, which lessens CF s severity and slows its progression, was just approved. ....

Sara Aldrich , Kim Steele , Errol Mcgihon Postmedia , Bruce Deachman , Postmedia Network Inc , Ontario Exceptional Access Program , Ontario Disability Support Program , Exceptional Access Program , Errol Mcgihon , Cystic Fibrosis Canada , Ontario Drug Benefit , Postmedia Network , Street East ,

DUPIXENT® (dupilumab injection) now publicly reimbursed in Ontario and New Brunswick for the treatment of moderate-to-severe atopic dermatitis

DUPIXENT® (dupilumab injection) now publicly reimbursed in Ontario and New Brunswick for the treatment of moderate-to-severe atopic dermatitis
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Marissa Poole , Kim Papp , Eczema Society Of Canada , Ontario Exceptional Access Program , Health Canada , Country Lead , Sanofi Canada , General Manager , Sanofi Genzyme , Ontario Exceptional Access , Eczema Area , Severity Index , New Brunswick Drug Plans , New Brunswick Drug Plans Formulary , Physician Global Assessment , Severity Score , Patient Care Atopic , Accessed May , Eczema Society , Atopic Dermatitis Quality , Canada Product , Atopic Dermatitis , Health Canada , New Brunswick , Ontario Exceptional Access Program , Biologic Medicine ,

Family pinning hopes on fundraisers for toddler's $2.8M treatment

Family pinning hopes on fundraisers for toddler s $2.8M treatment
A Pikwàkanagàn First Nation family is scrambling to raise millions of dollars for to provide a cure for their 14-month-old s genetic disorder, spinal muscular atrophy, before he turns two.
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Born with genetic disorder SMA2, Kevin Verch must receive one-time dose of Zolgensma before he turns 2
Posted: Jan 07, 2021 4:00 AM ET | Last Updated: January 7
Dana Pearce, 20, Brody Verch, 22, and their son Kevin Verch. The family is relying on fundraisers to pay for the toddler s $2.8-million genetic treatment for spinal muscular atrophy, which he must receive before he turns two in November. (Submitted by Dana Pearce) ....

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