Source Nutraceutical

SourceDirect.ca Launches New Site

Administrator — Tue, 15 May 2012 22:08:08 +0000

May 1st will mark Source Direct’s 8 year anniversary – and as part of this milestone, we are unveiling a fresh new look for Source Direct Design and Displays.

For design nerds like us, this is very exciting. Seeing people react to new branding is fascinating to watch. Comments have been overwhelmingly positive, and has injected our team with renewed energy, and drive. 2012 will be a big year for us as Source Direct, and we want you all to be a part of it.

We feel that the simplicity, and elegance of the new look is in line with our vision, and our passion to produce strong, memorable work. Not to mention, our ability to connect with our clientele, and exceed their expectations.

We know that this energy will keep our team, and yours inspired.

See the new site here >>

Source Nutraceutical to attend CHFA West

Administrator — Tue, 03 Apr 2012 09:03:42 +0000

Source Nutraceutical will be at the CHFA West Trade Show: Saturday, April 21 & Sunday, April 22, 2012

Where: Vancouver Convention Centre, West Building, Vancouver, BC

Western Canada’s largest natural health and organics trade event.

Category Specific Guidance for Temporary Marketing Authorization: Caffeinated Energy Drinks

Canadian Compliance Expert — Fri, 23 Mar 2012 18:11:59 +0000

In an announcement by the Minister of Health on October 6, 2011, Health Canada declared its intention to revise its classification of caffeinated energy drinks from natural health products to foods. Due to its public perception and history of use, product representation to consumers and product format, it was deemed by Health Canada that caffeinated energy drinks better fit the definition of a food. As a result, caffeinated energy drinks that have been granted NPNs or ENs, or products with Product Licence Applications that were submitted prior to October 6, 2011, are currently being shifted to the food regulatory framework, and this transition will be facilitated by the issuance of Temporary Marketing Authorization Letters (TMALs). TMALs will allow eligible caffeinated energy drinks to be marketed subject to specific conditions, until final regulatory requirements are put in place for these products in the Food and Drug Regulations.

In order to keep your caffeinated energy drink on the Canadian market, an application must be submitted to the Food Directorate for Temporary Marketing Authorization (TMA). In order to obtain TMA, certain eligibility criteria must be met such as restrictions on level of caffeine from all sources, levels of added vitamins, minerals and amino acids, and for novel ingredients and food additives. Additionally, the Food Directorate has put forth a series of requirements for labels, including quantitative and qualitative caffeine declarations, caution statements, quantitative declaration of other ingredients, and declaration of priority allergens.

Companies eligible to receive a TMAL must submit an application for Temporary Market Authorization of their caffeinated energy drink to the Food Directorate by April 30, 2012. Companies with products that do not meet compositional requirements are required to inform the Food Directorate no later than June 1, 2012 of their intention to reformulate the product. If you are unsure if your product is eligible to receive a TMAL based on its current formulation, please contact Source Nutraceutical for a comprehensive review of your product.

We can prepare your application for TMA of your caffeinated energy drink to help maintain your product on the Canadian market. We can also help you reformulate your product such that it meets the new composition requirements.

More complications with Natural Health Product Consulting and Packaging Compliance Canada

Administrator — Wed, 07 Mar 2012 20:15:44 +0000

New regulations concerning natural health products (NHPs) packaging are making it hard to enter the sector. To bring your NHPs to market in Canada, various regulations exist which impact the design of your packaging. Following the rules and regulations can be time consuming and difficult. Regulations are specific and stern, failure to comply with packaging regulations can have drastic effects upon your business and product.
The Canadian Natural Health Products Regulations (NHPR) are designed to foster fairness and uniformity in the Canadian market. As such, the responsibility falls on the producer to comply with regulations, it is imperative that the manufacturer completely understands the repeatedly changing policy, or seeks assistance of a trained professional. Certain regulations mandate bilingual packaging for instance. A product, which fails to comply with the labeling regulations, will be deemed unsafe for consumption, ultimately being pulled from sale across the country. Many companies are becoming more upset with the strict regulations and their impact on the industry. Ultimately, these complex loopholes prevent smaller companies, with fewer resources, from entering the market without extensive research, or professional help from compliance professionals.

Regulatory Affairs Winnipeg

Administrator — Tue, 28 Feb 2012 20:13:12 +0000

Are you trying to bring your organic products to market in the US or Canada? Some Winnipeg farmers found out how harsh regulations can be. Organic regulations are finely written rules that must be followed to the tee in order to achieve the seal of approval. The organic certificate benefits the farmer in many ways. Not only is an organic certified product healthier, its value is also increased in the Canadian and US market. A certified organic product also sends a statement about the quality and value to the consumer. The benefits can be worth the extra productions steps, even though the process seems very complicated.

Expert regulation specialists can aid farmers in every step of the way. Starting with the production, the specialists will review and correct standard operating procedures, inspect and prepare the facility, assist in managing records, and laboratory testing. The aid continues through compliant labeling and packing and extends all the way to a certification liaison.

Did you know? An organic logo can only be obtained through a government-approved certifier. It’s highly recommended to seek the aid of a professional when attempting to pass regulations; these professionals are experts in this field, removing any guess work with regulation compliance.

Natural Health Product Consulting and Packaging Compliance Canada

Administrator — Thu, 16 Feb 2012 20:14:59 +0000

Companies often face hardship when attempting to redesign their packaging while staying compliant with Canadian regulations. Detailed and complex regulations set a winding and difficult road to ensure your product is 100% ready for market. Regulations change and your current packaging may potentially be no longer compliant with new laws. Maybe you require a new look? Professional consultants can offer their knowledge to assist you in your quest for your natural health products (NHP).

Regulation compliance companies offer more than just consultation on staying within the law. Other services make up their business model as well, such as logo design and translation. A stunning package design plays a major role in a consumer’s choice at the time of purchase. Package consulting companies will work with their client to design a stunning presentation to put your product in the spot light, while still conveying the message you want to your consumers. Many businesses make the mistake of cutting costs by attempting to design their own logos and packaging. The end result is a product that doesn’t stand out and make a statement to potential consumers. Don’t make the same mistake, let a professional offer their guidance. Contact us if you need any help.

Natural Health Product Consulting and Packaging Compliance Canada

Administrator — Mon, 30 Jan 2012 20:13:59 +0000

When investing in natural health products (NHP), the time between investment and your product hitting store shelves is imperative. Many investors are unaware of the complicated and strict loopholes manufacturers face in packaging compliances. Most small businesses are ill equipped to deal with such a magnitude of strict guidelines and complications. The end result of attempting to correctly package your NHP product within compliance of regulations may take months, ultimately ending in failure. The slightest and smallest mistake could result in liability from upset or harmed consumers. Not to mention the negative spotlight your company could receive.

Well, consulting companies who specialize in packaging compliance are alive and well in Canada! Compliance consultants aren’t just useful for smaller business. Larger corporations routinely consult with compliance professionals to efficiently and quickly bring their new products to market while ensuring regulations are met. They recognize the importance of utilizing professionals to ensure 100% compliance as well as a quick turn around. In addition, consulting firms also routinely offer other packaging services perfect for small and large companies such as: design work, logo creation, translation services, nutritional information, and marketing services.

If you need any of the services above, be sure to chat with us.

Regulatory Affairs Winnipeg

Administrator — Tue, 24 Jan 2012 20:12:38 +0000

Regulatory affairs in Winnipeg, as well as the rest of Canada, are complicated and ever changing. New legislation is passed almost daily. Adherence to these regulations is imperative to maintaining consumer safety, as well as ethical business practices.

Regulation specialists ensure a consumer can happily consume a product, without unnecessary harm. A safe product is important for several reasons. Your brands name depends on the consumer’s association with a companies continued ethical responsibility to produce a safe product for consumption. Secondly, a safe compliant product allows legal entry into the market place. Finally, a safe product prevents liability suits from harming the consumer.

In the end, these strict regulations are all designed with the same goal in mind: protecting the happiness and livelihood of the consumer. These strict policies affect an enormous range of industries such as: pharmaceuticals, cosmetics, food & drink, packaging, organics products, and even dietary supplements.

Seeking the help of a regulation compliance specialist ensures your small company or corporation is legally and ethically adhering to regulations you may not even know exists. The end result is a safe product ready for market in Canada, while being fully compliant with any applicable regulations.

Source Nutraceutical – Canadian Compliance Consultants

Administrator — Tue, 10 Jan 2012 19:43:06 +0000

Regulations Update : Schedule F Changes

Canadian Compliance Expert — Thu, 08 Dec 2011 21:17:53 +0000

In 2009, NHPD began the scientific assessment of 11 naturally-sourced substances on Schedule F of the Food and Drug Regulations to determine if they could be regulated (in whole or in part) as nonprescription products under the Natural Health Product Regulations. As of December 7, 2011, 10 of those 11 substances are now eligible for pre-market review by the NHPD, depending on certain requirements.

1) Apiol, oil of, Deanol and its salts and derivatives, Theobromine and its salts and Centella asiatica extract and active principles thereof have been removed from Schedule F and are now allowed to have nonprescription status.

2) The Schedule F listing of Dopamine and its salts, Gold and its salts and Uracil and its salts have been amended to the following:

Dopamine and its salts, when sold for administration by injection.
Gold and its salts when sold for administration by injection.
Uracil and its salts when sold for the treatment of cancer.

For the above substances, all other dosage forms and routes of administration at any strength and for any use are exempt from prescription status.

3) The status of Dimethyl sulfoxide, Levocarnitine (L-carnitine) and its salts and derivatives and L-Tryptophan, have been revised to retain their prescription status as follows:

Dimethyl sulfoxide – for veterinary use, or when sold for the treatment of interstitial cystitis or scleroderma in humans.
Levocarnitine - when sold for the treatment of primary or secondary levocarnitine deficiency.
L-tryptophan, when sold:
- For human use in oral dosage form at a concentration of more than 220 mg per dosage unit or per daily dose, as a single ingredient or in combination with other ingredients; or
- For human or veterinary use as a single ingredient intended for any route of administration other than oral.

The proposed amendment to the Schedule F listing of Lovastatin is still under review by Health Canada.

For further information on this release, please contact Source Nutraceutical, Inc. at info@sourcenutra.ca.