Biopharmas have options to reduce cost profiles of R&D materials which can improve cash flow.
Key takeaways
Special tariff provisions and alternate customs values are two tariff and transactional tax-cost reduction strategies for R&D-stage products.
Biopharmas should analyze their clinical trials to determine any indirect tax optimization opportunities.
Biopharmaceutical companies contend with high costs when developing potential drug candidates, managing everything from a variety of clinical trial expenses to additional costs on customs tariffs and other indirect taxes such as value-added taxes or goods and services taxes.
Diving deeper into the topic of tariffs and taxes, many biopharmas assume that import tariffs and taxes are an inescapable cost of doing business and forego exploring savings opportunities. The reality is that companies do have options to reduce the cost profiles of their research and development (R&D) materials which can help improve cash flow.
Note the following:
Special tariff provisions
For clinical studies or other sorts of product development activities such as testing, evaluation or quality control taking place in the U.S., special tariff provisions exist to effectively eliminate otherwise applicable customs duties. The cost savings can be substantial when tariff rates of 5%, 10% or even 25% fall to zero. Not only can companies start capitalizing on the savings immediately going forward, they may also be able to recoup previously paid tariffs.
Alternate customs values
In the U.S. and globally, companies can apply other tariff cost-savings strategies such as lowering the declared customs value of the materials. For global clinical trials, companies must pay ad valorem import duties and indirect taxes based on a shipment’s commercial value. Since these investigational materials are not actually sold, it is often difficult to determine an acceptable value. In many instances, companies declare the products at a price point that is higher than necessary which means greater tariff and indirect tax costs. Some customs authorities appreciate that a drug’s per-unit production price should generally decrease once commercialized and fall further during its life cycle. Provided an analysis is performed and documented to defend the chosen method of merchandise appraisement for customs purposes (and supporting financial accounting records are well maintained), there is an opportunity to declare projected costs as the customs value for clinical materials.
Special tariff provisions and alternate customs values are just two tariff and transactional tax-cost reduction strategies for R&D-stage products. Alone, either strategy can help lower landed costs of clinical materials and alleviate some financial pressures in both early-stage and ongoing production activities internationally. Combined, they may give a company a significant and sustained advantage versus the competition through a lower operating cost profile and scalable savings.
Next steps
Biopharma companies should analyze their clinical trials to determine any indirect tax optimization opportunities. This endeavor should consider, at a minimum, the following:
- Location(s) of clinical trials
- Projected R&D expenditures over the next one to two years
- Tariff expenses on imported chemical compounds and clinical materials
- VAT and indirect tax expenses on imported chemical compounds and clinical materials
- Supportive customs appraisement analysis and declared import values
RSM contributors
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Jodi AderManager -
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