Trade groups and consumer advocates are working to fight the rising tide of protectionism generated by the coronavirus disease 2019 pandemic. The International Generic and Biosimilar Medicines Association (IGBA) is calling for dedicated air and sea channels to keep pipelines of essential medicines open between borders.
Aware that travel restrictions and border controls imposed by coronavirus disease 2019 (COVID-19) pose a threat to drug supply, the International Generic and Biosimilar Medicines Association (IGBA) is working to establish priority designations for medicines in air and sea cargo transport.
The move is among diverse attempts by private and public institutions recently to secure supplies of drugs and pharmaceuticals amid the dizzying pace of events. “The situation is constantly and rapidly changing,” said Suzette Kox, secretary general of IGBA, in an interview with The Center for Biosimilars®.
In recent days, many have spoken out against export curbs and other protectionist measures that threaten to upset the balance of international healthcare. Some actions by governments have involved instating emergency powers to bypass patent exclusivity protections where necessary.
On March 25, the Canadian legislature passed an emergency bill that would allow that country to circumvent patent laws to ensure adequate supplies that are needed to respond to the COVID-19 public health emergency.
And White House administration trade advisor Peter Navarro recently stated publicly that the administration was planning to order federal agencies to prioritize purchasing US-made drugs and medical supplies.
IGBA Cautions About Export Restrictions
The IGBA contends that any restrictions on the export of pharmaceutical products are counterproductive. “We will work toward keeping global markets open, and our industries are focusing right now on meeting the increasing demands. We also see encouraging signs of international commitments, collaboration, and coordination to support the movement of medicines,” Kox said.
The group today called for governments gobally to establish priority designation for medicines at custom controls and for cargo and freight. The priority would include goods needed to manufacture these agents.
“There is an absolute urgency to facilitate and speed up the movement of essential products at all levels, in particular at customs control, as well as systematically reserve cargo capacity for those products in air/sea cargo, which are vital partners in delivering much-needed essential goods,” the group said in a release.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Can Global Policies to Boost Biosimilar Adoption Work in the US?
November 17th 2024On this special episode of Not So Different honoring Global Biosimilars Week, Craig Burton, executive director of the Biosimilars Council, explores how global policies—from incentives to health equity strategies—could boost biosimilar adoption in the US.
Subcutaneous Infliximab CT-P13 Superior to Placebo as Maintenance Therapy for IBD
November 16th 2024In 2 randomized controlled trials of maintenance therapy for inflammatory bowel disease (IBD), the subcutaneous formulation of the infliximab biosimilar CT-P13 demonstrated superiority to placebo in patients with Crohn disease and ulcerative colitis.