Learn how to navigate the challenges posed by rising interest rates and inflation on equipment financing. Get practical tips and strategies to manage the impacts and ensure your business can secure cost-effective equipment financing.
July 2023
Gain an understanding of the world of operating expenses (OpEx) with this informative blog post. Learn about OpEx and its significance in managing and evaluating business costs.
July 2023
Dive into the world of FMV leases in this informative blog post, where we define this leasing option and provide real-life examples. Gain insights into how FMV leases work and the advantages they offer.
July 2023
Read about the tax advantages of equipment leasing and explore how leasing can help optimize your business's tax strategy, reduce upfront costs, and potentially provide tax deductions. Maximize your financial benefits with equipment leasing.
July 2023
Learn about CapEx in this informative blog post. Gain clarity on what capital expenditures are, explore practical examples, and understand their vital role in business operations and long-term growth strategies.
July 2023
Learn about the fundamentals of capital leases in our comprehensive guide. Explore the ins and outs of capital lease agreements and learn about the advantages they offer businesses.
July 2023
Biotechnology podcasts have emerged as a powerful medium for professionals to stay informed about the latest developments and trends in this fast-moving industry. Looking for a biotech podcast to listen to? Learn more here.
April 2023
What is the FDA and its drug approval process? Founded in 1930, the US Food and Drug Administration (FDA) is responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs and more.
March 2023
Established in 1906, the FDA regulates food and drug safety. The 1938 Act broadened its role, approving new drugs based on safety and efficacy. NDAs, submitted for marketing new drugs, require comprehensive data on safety, efficacy, and more.
March 2023
An Abbreviated New Drug Application (ANDA) is a regulatory submission to the US FDA for generic drugs. It demonstrates that a proposed generic drug is the same as an approved reference listed drug (RLD) in terms of safety, efficacy, and quality.
March 2023
