Key Questions to Ask When Ordering Intermediates Pharma Service

As a bio/pharma API sourcing partner there are two straightforward questions we hear from clients:

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1. When we can receive the API in the quantity we desire?
2. What will be the cost?

Our answers to these two questions are invariably the same: it depends.

While disappointing as far as answers go, it’s also the correct one. Answering those two questions will always require more information than most companies expect – and the scope of that information is sometimes eye-opening for newer sourcing and procurement professionals. The fact is, there are many factors that come into play when you engage with drug substance suppliers, and all of them must be taken into consideration.

The key thing pharma execs must remember is that everything hinges on the business case. Yes – of course there are API or intermediate suppliers who will shrug and say, “an order is an order…sure we’ll fill it.” But there are fewer of those than you may think. Drug substance manufacturers will likely ask a litany of questions before they consider entering into a supply agreement. They need to ensure this relationship makes sense for their business.

In smaller and virtual biopharma companies, the answers to supplier questions may be difficult to come by. In virtual or very early-stage companies (think “two brains and a molecule”), some supplier queries have answers, but the company may not want to share them…either with the sourcing company or the potential supplier. In other cases, the project may not have matured knowledge-wise to a point where long-range projections are available.

API Sourcing Questions You Need to Be Prepared to Answer

A sourcing partner like LGM will ask you questions beyond ‘when’ or ‘how much.’ We aren’t being nosy. We promise! But any supply relationship we create for you, or you form on your own will likely depend on your answers…and your willingness to answer.

With that said, here are some of the topic areas a supplier will want to explore when considering whether to participate in your drug project.

The Basics

1. What’s the indication?
2. What’s the drug’s route of administration?
3. Will the API or drug substance require any special handling or transport, or pose any other kind of logistics challenge?
4. How complex is the chemistry? How developed is it? What is the basic approach (antibody drug conjugate, a deuterated small molecule, a peptide via solution phase synthesis)?

Beyond the basics, there are some broader topic areas a supplier will want to explore. Here are 5 more areas API manufacturers want to explore before you become a client.

5. Non-GMP Research or GMP Clinical Material?
   Will you initially need any non-GMP material for research or experimental purposes, or will you only want GMP material? Non-GMP material will clearly cost less, and may offer opportunities to find an API supplier that isn’t FDA inspected, or doesn’t work with as many GMP substances.Timing comes into play, as well. If you will be transitioning from non-GMP to GMP material in short order or will need additional GMP material in the next few months, then it is worth the extra investment to find a longer-term supplier upfront.Generally, it is not wise to begin a project with a non-GMP supplier only to realize they will not be able to support you when higher quality materials are necessary.

6. Geography
   Which markets will you be targeting? Some suppliers may have only specific geographies available for purchase, due to prior exclusivities or other agreements they already have in place.Aside from any exclusivities or restrictions, the target geography is important because it indicates which regulatory standards will apply during manufacture. Will APIs need to comply with US Pharmacopoeia, for example, or meet EU EMA, US FDA or other global standards?Geographically speaking, your suppliers need to match the requirements of your current and future target markets.

7. Regulatory Pathway
   The regulatory pathway you will be choosing for your drug candidate will have a big impact on supplier selection and availability. For example, pursuing an NDA has different requirements (and a much longer pathway) than a 505(b)(2) or an OTC compound.Generic and OTC APIs have their own challenges. While there are many more suppliers, margins are very low, and volumes matter.

8. Quantity
   Speaking of volumes mattering…they really As a biopharma company you may be looking for security of supply but remember suppliers are looking for security of revenue.A one-off RFQ for an R&D quantity of a difficult-to-make API will have fewer takers…and most will be requesting projections, forecasts and timelines for future quantities.You may need 100 grams for R&D and evaluation, but what’s your plan? When will you need quantities for submission batches? What is your high-level estimation of what you will need at kg scales? How many metric tons?

   This is what the manufacturer wants to get to…a situation in which they have a long-term relationship build around a commercially viable compound. If they will be allocating resources and manpower to this drug substance, they want to manage their business risk as much as possible.

9. First, Primary or Secondary Source
   Suppliers will want to know whether you are looking for the initial source of a drug substance, or a primary or secondary supplier. It isn’t uncommon for companies to be reluctant to disclose they already have a source – or whether they are evaluating a second source for savings, quality improvements, or to build risk mitigation into their supply chain.As a sourcing partner to biopharma companies, we’ve run into situations where not knowing this upfront led to problems. In one particular case, we approached a manufacturer for a quote only to be told they had been working with the company directly as the primary supplier for nearly four years!

The Answers We Don’t Have Can Make a Difference.
We know molecules – and we know how to find them for biopharma companies. Much as suppliers will want to know answers to some key questions, when we have this information we can better refine our lists of potential suppliers and zero in on the best solution for our drug company clients.

Are you interested in learning more about Intermediates Pharma Service? Contact us today to secure an expert consultation!

Active pharmaceutical ingredients (APIs) are the active components in a pharmaceutical drug that produce the required effect on the body to treat a condition. APIs are produced by processing chemical compounds. In a biologic drug, the active ingredient is known as a bulk process intermediate (BPI).

Despite high manufacturing expenses, strict regulatory policies, and policies in controlling drug prices in many countries, attractive opportunities have emerged in the API market due to growing cases of chronic diseases, including diabetes, asthma and cancer.

The information provided in the download document is drafted for pharmaceutical executives, research and development (R&D) executives, quality control and quality assurance executives, as well as API manufacturers, distributors, suppliers, sales managers, process engineers, technicians, research associates and production chemists, and any other individuals involved in the operations of the API and active pharmaceutical intermediates industry.

The download contains detailed information on API manufacturers to aid in purchasing decisions, including product ranges and contact details.

Related Buyer’s Guides which cover an extensive range of pharmaceutical technologies, equipment, and manufacturers, can also be found here.

Types of active pharmaceutical ingredients

APIs are broadly categorised into two types – synthetic and natural. Synthetic APIs are further classified into innovative and generic synthetic APIs, based on the type of synthesis used.

Synthetic chemical APIs, also known as small molecules, constitute a large part of the pharmaceutical market, with many small molecule drugs commercially available in the market.

Natural APIs are used in making biologics, which are increasingly becoming the top-selling drugs in the market. Despite the growing demand, biologics are currently significantly fewer in number compared to small molecule drugs.

Based on the solubility, APIs are categorised into insoluble and soluble drugs.

Top active pharmaceutical ingredients and intermediates suppliers

Pharmaceutical Technology has listed the leading suppliers of active pharmaceutical ingredients and intermediates based on its intel, insights and decades-long experience in the sector. The list includes companies that can develop and supply high-quality pharmaceutical materials, including, but not limited to:

• Fine chemicals and intermediates, such as high-docosahexaenoic acid oil for API production
• APIs for central nervous system therapies
• Natural cannabinoid (CBD) ingredients, CBD isolates and cannabis distillates
• Excipients
• Insulin for cell culture media
• Ammonium compounds
• Mineral salts

The list also includes suppliers of mixing and drying technologies, polymer coatings for drug delivery, extraction technologies for high-purity APIs, and dispersion and wet milling technology. Providers of automatic capsule filling machines, dry powder and liquid-based material handling systems, analytic services for biological assays, pharma tablet manufacturing machines, and custom synthesis services are detailed in the document as well.

If you are looking for more details, kindly visit Drug Substance CDMO Services.

For full details (including contact details) on the leading companies within this space, download the free Buyer’s Guide below: