No. Customers are responsible for providing their own labels. We have close relationships with several printers that have many clients in the nutraceutical industry, to which we can refer you.
Yes, provided they comply with the raw material agreed specifications between you and Rhema and any necessary indemnities are in place.
We manufacture effervescent powders in bulk for outsourced filling in appropriate oxygen barrier packaging. We do not presently manufacture effervescent tablets.
We conduct in-house organoleptic (colour and smell) testing of all raw materials as well as testing specific to the manufacturing process such as weight checks, disintegration, hardness and friability. All other testing including microbial, heavy metals analysis and chemical analysis (identification and potency assay), as well as testing for solvent and pesticide residues is conducted by 3rd party government certified laboratories. Any additional testing requirements can be discussed with your Account Executive in conjunction with our Operations team.
We have greater than doubled our capacity through the purchase of our US facility and the addition of a two tonne ribbon blender. Our move to new larger premises for packaging in the US is a further testament to our commitment for growth. We continue to build capacity in our other dosage forms as required and have expanded our capabilities to include sachets, stick-packs and soft plastic gusset bags. Many of our customers have experienced continuous double digit growth including periods of explosive growth, and we have consistently been able to keep pace with their needs. When you partner with Rhema for your manufacturing and packaging needs, you can rest assured that we have planned for growth and have the experience to handle the welcome challenges that accompany your growth.
We manufacture and package powders, capsules and tablets from our headquarters in British Columbia, Canada. We manufacture and package powders in Utah, USA. We are able to package powders in jars, canisters, sachets, stickpacks, gusset bags, tablets and capsules in our Canadian facility and jars, canisters, sachets and gusset bags in our US facility.
Yes. Certificates of Analysis are provided according to the parameters defined in the Finished Product Specification.
No, we do not offer fulfillment services. We have close relationships with several fulfillment locations that have clients in the nutraceutical industry, to which we can refer you.
We manufacture to the quantity of your purchase order. We do not store excess finished goods for our customers.
Pricing is calculated based on the current landed cost of each material. Given the dynamic nature of the industry, component pricing can fluctuate rapidly. Accordingly, quotations are valid for 30 days and must be re-quoted if an order is not placed during that timeframe. We recommend that you approve your quotation and place your order immediately after approving the quotation as this will secure your price for that production run and will be most efficient for all parties.
Before a production batch is conducted, we evaluate the physical properties of the ingredients for parameters such as flowability and density as well as particle size and shape. Our team of technical experts makes a determination whether the ingredients can be mixed dry or whether wet granulation is required and in what type of blenders the ingredients will be mixed. We also consider other factors such as the time required for blending without causing particle separation or over mixing, the fill level of the blender, and the order of adding each ingredient.
When required, we employ various processes to prepare the ingredients for blending, compression or encapsulation.
Some of the processes we utilize to bring materials into a production-ready state include:
- Milling, which will provide a consistent particle size
- Granulation, which will form granules
- Chilsonation, which will increase density
- Trituration, which will intersperse the actives in a diluent to increase the surface area of the actives
Ideally, all materials would be received already in a free-flowing, production-ready state; however this is not always possible. When materials are difficult to work with, you can rely on Rhema’s experience, quality and innovation to find the best manufacturing solution.
The turn-around on a quotation depends on many factors. First, our formulators review your formula to determine whether it will achieve your desired product parameters or they develop a formula from your product concept. Often there are several iterations required to fine tune and arrive at a final formula. Once the formula is finalized it is sent to our costing department to create a cost estimate. The estimate is based on the price of the raw materials, production costs, and packaging costs, if applicable. If the formula has a large number of materials or the materials are particularly unusual or unique we will need to confirm current pricing with our raw material suppliers or find a source for the new materials and obtain pricing and specifications. Once the cost estimate is complete, it is reviewed by the appropriate departments before being sent to your Rhema Account Executive for final review and quotation. The process of creating a formula, cost estimate and quotation can take as little as one to two days or up to three weeks. When you request a price your Rhema Account Executive can give you an approximate timeline for quoting on your formula.
Lead times vary significantly based on many factors, including:
- the complexity of the product(s) and availability of the raw materials
- the number of products required
- whether product development is required
- the QC testing required
- whether products are being produced for the first time or are repeat orders
- whether they are to be shipped in bulk or packaged
- what our existing production commitments are at the time you place your order
Products being produced for the first time that require extensive product development require a 6 month lead-time to finished product; this represents roughly a 10-12 week development process followed by a 12 – 14 week production schedule.
Typical lead times for repeat orders vary depending on the availability of the raw materials. We require 6 – 8 weeks from the time of receipt of all raw materials to produce a quality tested, finished product with accompanying certificate of analysis. Speak to your Account Executive regarding other documentation you may require.
Other factors that can affect lead time are the timing of your sign-off on the Rhema sales order, any required deposit or receipt of your labels and other packaging components.
Powder: 500 kg
Capsules: 200,000 capsules
Tablets: 200,000 tablets
Coating: 150 kg of tablets/capsules/softgels
Minimum order requirements are negotiable for certain products. Ask your Rhema Account Executive for further details.
We provide a Certificate of Analysis, Commercial Invoice and a Packing Slip. If you require any additional documentation, these requirements must be identified on the sales order.
Rhema manufactures exclusively dry dosage forms, specifically 2-piece hard shell gelatin or vegetarian capsules, powders, and tablets including chewables, lozenges and sub-linguals. We also offer a proprietary GRAS-affirmed aqueous based enteric coating for soft gelatin capsules and tablets, as well as standard coating for tablets to produce an aesthetically pleasing shiny appearance and to facilitate ease of swallowing, and delayed-release coating enabling products to release activity for up to a six hour period.
Rhema packages powders, tablets, capsules and soft-gelatin capsules.
- Certified GMP compliant and Establishment licensed (# 100228-A) by Health Canada for the fabrication and packaging of drug (DIN) products.
- Site licensed (# 300704) for natural health products (NHP).
- Precursor A licensed (# 9-0291-2010) for the manufacture and packaging of ephedrine and pseudo-ephedrine.
- NSF and NSF for Sport Certified in the US
- TGA approved for the fabrication of therapeutic goods in Australia.
- The FDA issued an Establishment Inspection Report in July 2011 to RHPL for Food and Dietary Supplements, and no FDA 483 Report was filed
- Organic certified through QMI (1621868) for the manufacture and packaging of specific organic products.
- We can obtain kosher certification for specific production runs, as required.
We offer: blending of powders, encapsulation in 2-piece gelatine or vegetable capsules, coating and enteric coating for tablets and soft-gelatin capsules and packaging and labelling. Our powder filling capabilities include jars and canisters, single-dose stick packs and sachets as well as soft plastic gusset bags. We are also able to fill multiple tablets and capsules into cellophane single-dose packets.
We manufacture with capsules (gelatin or vegetarian) in the following sizes organized from smallest to largest:
#3, #2, #1, “0” and “00”.
We manufacture tablets in a wide range of sizes and shapes including: ¼” round to 7/8” round, ½” X ¼” caplet, ¾” X 5/16” caplet, 5/8” X 5/16” oval, 7/8” X 3/8” oval and many more.
We will work with you to size your product appropriately. Unique punches and capsule printing is available at a premium.